Canonical Allele Identifier: CA407414555

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889990-C-A
• MyVariant Identifiers: chr19:g.54393244C>A (hg19) ; chr19:g.53889990C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889990C>A , CM000681.2:g.53889990C>A	GRCh38
NC_000019.9:g.54393244C>A , CM000681.1:g.54393244C>A	GRCh37
NC_000019.8:g.59085056C>A	NCBI36
NG_009114.1:g.12778C>A , LRG_669:g.12778C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.502C>A	ENSP00000507230.1:p.Pro168Thr
ENST00000682268.1:n.800C>A
ENST00000682902.1:n.804C>A
ENST00000683513.1:c.502C>A	ENSP00000506809.1:p.Pro168Thr
ENST00000263431.4:c.502C>A MANE Select	ENSP00000263431.3:p.Pro168Thr
ENST00000263431.3:c.502C>A	ENSP00000263431.3:p.Pro168Thr
ENST00000474397.5:c.118C>A	ENSP00000471271.1:p.Pro40Thr
NM_001316329.1:c.502C>A	NP_001303258.1:p.Pro168Thr
NM_002739.3:c.502C>A , LRG_669t1:c.502C>A	NP_002730.1:p.Pro168Thr
NM_002739.4:c.502C>A	NP_002730.1:p.Pro168Thr
NM_002739.5:c.502C>A MANE Select	NP_002730.1:p.Pro168Thr
NM_001316329.2:c.502C>A	NP_001303258.1:p.Pro168Thr