Human (GRCh38.p14)
Description

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

About this transcript

This transcript has 2 exons, is annotated with 21 domains and features, is associated with 2103 variant alleles and maps to 383 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: 2, Coding exons: 1, Transcript length: 3,617 bps, Translation length: 324 residues

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:2

Version

ENST00000514199.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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