Description

sodium channel, voltage-gated, type XI, alpha subunit [Source:HGNC Symbol;Acc:HGNC:10583]

Synonyms

NaN, Nav1.9, SCN12A, SNS-2

Location
INSDC coordinates

chromosome:GRCh38:CM000665.2:38845769:38950561:1

Transcripts



This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
SCN11A-001ENST0000030232865001791 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS33737Q9UI33 NM_001287223
NM_014139
NP_001274152
NP_054858
TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PIAPPRIS principal isoform [01-09-2014]
Glossary entry for APPRIS
APPRIS website
SCN11A-002ENST0000044423757291444 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-Q9UI33 -TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
SCN11A-003ENST0000045622452621753 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-Q9UI33 -TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

Gene-based displays