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 6 exons, is associated with 2686 variant alleles and maps to 231 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000221485.8SLC17A7-2012949560aaENSP00000221485.2
 
Protein coding
CCDS12764Q9P2U7-1 NM_020309.4MANE SelectEnsembl CanonicalGENCODE 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: 6, Coding exons: 0, Transcript length: 2,785 bps,

Transcript Support Level (TSL)

TSL:2

Version

ENST00000598018.1

Type

Retained intron

Annotation Method

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