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Human (GRCh38.p14)
Description

solute carrier family 17 member 7 [Source:HGNC Symbol;Acc:HGNC:16704]

Gene Synonyms

BNPI, VGLUT1

Location
About this transcript

This transcript has 12 exons, is annotated with 43 domains and features, is associated with 6420 variant alleles and maps to 584 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000221485.8SLC17A7-2012949560aaENSP00000221485.2
 
Protein coding
CCDS12764Q9P2U7-1 NM_020309.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000600601.5SLC17A7-2042237493aaENSP00000470338.1
 
Protein coding
Q9P2U7-2 -GENCODE BasicTSL:2
ENST00000596689.1SLC17A7-202553116aaENSP00000472086.1
 
Nonsense mediated decay
M0R1S5 -TSL:4CDS 5' incomplete
ENST00000598018.1SLC17A7-2032785No protein-
 
Retained intron
--TSL:2
ENST00000600672.5SLC17A7-2052024No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 12, Coding exons: 12, Transcript length: 2,949 bps, Translation length: 560 residues

MANE

This MANE Select transcript contains ENSP00000221485 and matches to NM_020309.4 and NP_064705.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9P2U7

CCDS

This transcript is a member of the Human CCDS set: CCDS12764

Transcript Support Level (TSL)

TSL:1

Version

ENST00000221485.8

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.

GENCODE primary gene

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