Human (GRCh38.p14)
Description

solute carrier family 30 member 7 [Source:HGNC Symbol;Acc:HGNC:19306]

Gene Synonyms

ZNT7, ZNTL2

About this transcript

This transcript has 11 exons, is annotated with 45 domains and features, is associated with 34575 variant alleles and maps to 657 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000357650.9SLC30A7-2018204376aaENSP00000350278.4
 
Protein coding
CCDS776Q8NEW0 NM_133496.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000370112.8SLC30A7-2037898376aaENSP00000359130.4
 
Protein coding
CCDS776Q8NEW0 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000886082.1SLC30A7-2052162156aaENSP00000556141.1
 
Protein coding
--GENCODE Basic
ENST00000370111.4SLC30A7-20262387aaENSP00000359129.4
 
Protein coding
H0Y362 -TSL:5CDS 5' incomplete
ENST00000850622.1SLC30A7-2042029376aaENSP00000520907.1
 
Nonsense mediated decay
CCDS776---
Statistics

Exons: 11, Coding exons: 11, Transcript length: 8,204 bps, Translation length: 376 residues

MANE

This MANE Select transcript contains ENSP00000350278 and matches to NM_133496.5 and NP_598003.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8NEW0

CCDS

This transcript is a member of the Human CCDS set: CCDS776

Transcript Support Level (TSL)

TSL:1

Version

ENST00000357650.9

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

alternative 3' UTR [Definitions]

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.