Human (GRCh38.p14)
Description

arylsulfatase D [Source:HGNC Symbol;Acc:HGNC:717]

Gene Synonyms

ASD

Location
About this transcript

This transcript has 10 exons, is annotated with 17 domains and features, is associated with 9744 variant alleles and maps to 835 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000381154.6ARSD-2025145593aaENSP00000370546.1
 
Protein coding
CCDS35196P51689-1 NM_001669.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000458014.1ARSD-203580159aaENSP00000409180.1
 
Protein coding
H7C327 -TSL:3CDS 5' incomplete
ENST00000559324.1ARSD-20756782aaENSP00000453789.1
 
Nonsense mediated decay
H0YMY1 -TSL:4
ENST00000217890.10ARSD-2012160No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000495294.1ARSD-2062032No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000481340.1ARSD-204352No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000494870.5ARSD-205663No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 10, Coding exons: 10, Transcript length: 5,145 bps, Translation length: 593 residues

MANE

This MANE Select transcript contains ENSP00000370546 and matches to NM_001669.4 and NP_001660.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P51689

CCDS

This transcript is a member of the Human CCDS set: CCDS35196

Transcript Support Level (TSL)

TSL:1

Version

ENST00000381154.6

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.