Description

arylsulfatase family, member I [Source:HGNC Symbol;Acc:HGNC:32521]

Synonyms

FLJ16069, SPG66

INSDC coordinates

chromosome:GRCh38:CM000667.2:150296343:150339307:1

Transcripts



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

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
ARSI-001ENST000003286683161569 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS34275D6RDH0 Q5FYB1 NM_001012301
NP_001012301
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 [01-09-2014]
Glossary entry for APPRIS
APPRIS website
ARSI-002ENST000005153011429426 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D6RDH0 Q5FYB1 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:4

TSL4:The best supporting EST for this transcript is flagged as suspect.

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.

ARSI-003ENST0000050914647286 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D6RDH0 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:4

TSL4:The best supporting EST for this transcript is flagged as suspect.

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.

Gene-based displays