Human (GRCh38.p14)
Description

FXYD domain containing ion transport regulator 7 [Source:HGNC Symbol;Acc:HGNC:4034]

Location
About this transcript

This transcript has 6 exons, is annotated with 11 domains and features, is associated with 5660 variant alleles and maps to 230 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000270310.7FXYD7-20170880aaENSP00000270310.2
 
Protein coding
CCDS12446P58549 NM_022006.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000968511.1FXYD7-20782182aaENSP00000638570.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000968512.1FXYD7-20870552aaENSP00000638571.1
 
Protein coding
--GENCODE Basic
ENST00000900287.1FXYD7-20569072aaENSP00000570346.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000934123.1FXYD7-20664569aaENSP00000604182.1
 
Protein coding
--GENCODE BasicAPPRIS ALT2
ENST00000588265.1FXYD7-204636117aaENSP00000465784.1
 
Protein coding
K7EKU3 -GENCODE PrimaryGENCODE BasicTSL:2
ENST00000968513.1FXYD7-20960652aaENSP00000638572.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000586063.5FXYD7-20345677aaENSP00000466915.1
 
Protein coding
K7ENE8 -GENCODE BasicAPPRIS ALT1TSL:3
ENST00000439441.1FXYD7-2021111No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 6, Coding exons: 6, Transcript length: 708 bps, Translation length: 80 residues

MANE

This MANE Select transcript contains ENSP00000270310 and matches to NM_022006.2 and NP_071289.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P58549

CCDS

This transcript is a member of the Human CCDS set: CCDS12446

Transcript Support Level (TSL)

TSL:1

Version

ENST00000270310.7

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.