Description

Nance-Horan syndrome (human) [Source:MGI Symbol;Acc:MGI:2684894]

INSDC coordinates

chromosome:GRCm38:CM001013.2:161833296:162159730:1

Transcripts



This gene has 2 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Nhs-001ENSMUST0000008708588051647 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS72461B1AV60 NM_001290526
NP_001277455
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

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).
Nhs-201ENSMUST0000008156948811626 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS41201B9EJX2 NM_001081052
NP_001074521
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

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 [04-09-2014]
Glossary entry for APPRIS
APPRIS website

Gene-based displays