Human (GRCh38.p14)
Description

solute carrier family 6 member 19 [Source:HGNC Symbol;Acc:HGNC:27960]

Gene Synonyms

B0AT1

Location
About this transcript

This transcript has 12 exons, is annotated with 44 domains and features, is associated with 13588 variant alleles and maps to 627 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000304460.11SLC6A19-2015168634aaENSP00000305302.10
 
Protein coding
CCDS34130Q695T7 NM_001003841.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000515652.5SLC6A19-2023337354aaENSP00000425701.1
 
Nonsense mediated decay
E9PD72 -TSL:2
Statistics

Exons: 12, Coding exons: 12, Transcript length: 5,168 bps, Translation length: 634 residues

MANE

This MANE Select transcript contains ENSP00000305302 and matches to NM_001003841.3 and NP_001003841.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q695T7

CCDS

This transcript is a member of the Human CCDS set: CCDS34130

Transcript Support Level (TSL)

TSL:1

Version

ENST00000304460.11

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.