Canonical Allele Identifier: CA2576907860

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900517-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900517C>A , CM000681.2:g.53900517C>A	GRCh38
NC_000019.9:g.54403771C>A , CM000681.1:g.54403771C>A	GRCh37
NC_000019.8:g.59095583C>A	NCBI36
NG_009114.1:g.23305C>A , LRG_669:g.23305C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1436+36C>A	ENSP00000507230.1:n.1436+36C>A
ENST00000682268.1:n.1734+36C>A
ENST00000682676.1:n.837+36C>A
ENST00000682902.1:n.1738+36C>A
ENST00000683513.1:c.1436+36C>A	ENSP00000506809.1:n.1436+36C>A
ENST00000263431.4:c.1436+36C>A MANE Select	ENSP00000263431.3:n.1436+36C>A
ENST00000263431.3:c.1436+36C>A	ENSP00000263431.3:n.1436+36C>A
NM_001316329.1:c.1436+36C>A	NP_001303258.1:n.1436+36C>A
NM_002739.3:c.1436+36C>A , LRG_669t1:c.1436+36C>A	NP_002730.1:n.1436+36C>A
NM_002739.4:c.1436+36C>A	NP_002730.1:n.1436+36C>A
XM_011527108.1:c.527+36C>A	XP_011525410.1:n.527+36C>A
NM_002739.5:c.1436+36C>A MANE Select	NP_002730.1:n.1436+36C>A
NM_001316329.2:c.1436+36C>A	NP_001303258.1:n.1436+36C>A