Human (GRCh38.p14)
Description

parvin gamma [Source:HGNC Symbol;Acc:HGNC:14654]

Location

Chromosome 22: 44,172,956-44,219,533 forward strand.

GRCh38:CM000684.2

About this gene

This gene has 12 transcripts (splice variants), 191 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000444313.8PARVG-2063488331aaENSP00000391583.2
 
Protein coding
CCDS14057Q9HBI0-1 NM_022141.7MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000422871.5PARVG-2053462331aaENSP00000391453.1
 
Protein coding
CCDS14057Q9HBI0-1 -GENCODE basicAPPRIS P1TSL:5
ENST00000415224.5PARVG-202999187aaENSP00000416761.2
 
Protein coding
Q9HBI0-3 -GENCODE basicTSL:2
ENST00000466375.2PARVG-20882034aaENSP00000475593.1
 
Protein coding
U3KQ67 -GENCODE basicTSL:2
ENST00000417767.1PARVG-20462230aaENSP00000407199.1
 
Protein coding
B0QYN0 -TSL:2CDS 3' incomplete
ENST00000416291.5PARVG-20330926aaENSP00000399839.1
 
Protein coding
B0QYM9 -TSL:3CDS 3' incomplete
ENST00000356909.7PARVG-2011425187aaENSP00000349378.3
 
Nonsense mediated decay
Q9HBI0-3 -TSL:5
ENST00000453888.7PARVG-207960No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000472551.1PARVG-211551No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000468564.6PARVG-2095066No protein-
 
Retained intron
--TSL:5
ENST00000475485.6PARVG-2122614No protein-
 
Retained intron
--TSL:5
ENST00000471836.1PARVG-210566No protein-
 
Retained intron
--TSL:4