Human (GRCh38.p14)
Description

solute carrier family 38 member 8 [Source:HGNC Symbol;Acc:HGNC:32434]

Gene Synonyms

SNAT8

Location
About this transcript

This transcript has 11 exons, is annotated with 15 domains and features, is associated with 29330 variant alleles and maps to 279 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000299709.8SLC38A8-2011672435aaENSP00000299709.3
 
Protein coding
CCDS32495A6NNN8 NM_001080442.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000568178.1SLC38A8-203861262aaENSP00000457737.1
 
Protein coding
H3BUP5 -TSL:5CDS 3' incomplete
ENST00000569816.1SLC38A8-20457846aaENSP00000455085.1
 
Protein coding
H3BP02 -TSL:4CDS 3' incomplete
ENST00000568003.1SLC38A8-202501No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 11, Coding exons: 10, Transcript length: 1,672 bps, Translation length: 435 residues

MANE

This MANE Select transcript contains ENSP00000299709 and matches to NM_001080442.3 and NP_001073911.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A6NNN8

CCDS

This transcript is a member of the Human CCDS set: CCDS32495

Transcript Support Level (TSL)

TSL:5

Version

ENST00000299709.8

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.

Annotation Attributes

inferred exon combination [Definitions]

upstream ATG

GENCODE basic gene

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