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Human (GRCh38.p14)
Description

solute carrier family 17 member 2 [Source:HGNC Symbol;Acc:HGNC:10930]

Gene Synonyms

NPT3

Location
About this transcript

This transcript has 12 exons, is annotated with 38 domains and features, is associated with 7540 variant alleles and maps to 475 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000377850.8SLC17A2-2032498478aaENSP00000367081.3
 
Protein coding
CCDS69060O00624-3 NM_001286123.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00000360488.7SLC17A2-2022270436aaENSP00000353677.3
 
Protein coding
CCDS4567O00624-2 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000265425.3SLC17A2-2011493439aaENSP00000265425.3
 
Protein coding
O00624-1 -GENCODE PrimaryGENCODE BasicTSL:5
Statistics

Exons: 12, Coding exons: 11, Transcript length: 2,498 bps, Translation length: 478 residues

MANE

This MANE Select transcript contains ENSP00000367081 and matches to NM_001286123.3 and NP_001273052.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: O00624

CCDS

This transcript is a member of the Human CCDS set: CCDS69060

Transcript Support Level (TSL)

TSL:5

Version

ENST00000377850.8

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 transcript model [Definitions]

RNA-Seq supported only

GENCODE basic gene

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

GENCODE primary gene

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