Human (GRCh38.p14)
Description

solute carrier family 35 member A4 [Source:HGNC Symbol;Acc:HGNC:20753]

About this transcript

This transcript has 3 exons, is annotated with 21 domains and features, is associated with 2153 variant alleles and maps to 346 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000323146.8SLC35A4-2012666324aaENSP00000327133.3
 
Protein coding
CCDS4231Q96G79-1 NM_080670.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000514199.1SLC35A4-2023617324aaENSP00000424566.1
 
Protein coding
CCDS4231Q96G79-1 -GENCODE basicAPPRIS P1TSL:2
ENST00000612662.2SLC35A4-2032789324aaENSP00000479255.1
 
Protein coding
CCDS4231Q96G79-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000623481.3SLC35A4-2041065103aaENSP00000485218.1
 
Protein coding
CCDS93794L0R6Q1-1 -GENCODE basicTSL:1
Statistics

Exons: 3, Coding exons: 1, Transcript length: 2,666 bps, Translation length: 324 residues

MANE

This MANE Select transcript contains ENSP00000327133 and matches to NM_080670.4 and NP_542401.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96G79

CCDS

This transcript is a member of the Human CCDS set: CCDS4231

Transcript Support Level (TSL)

TSL:1

Version

ENST00000323146.8

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.