Canonical Allele Identifier: CA2576907876

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900822C>A , CM000681.2:g.53900822C>A	GRCh38
NC_000019.9:g.54404076C>A , CM000681.1:g.54404076C>A	GRCh37
NC_000019.8:g.59095888C>A	NCBI36
NG_009114.1:g.23610C>A , LRG_669:g.23610C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+73C>A	ENSP00000507230.1:n.1575+73C>A
ENST00000682268.1:n.1873+73C>A
ENST00000682676.1:n.976+73C>A
ENST00000682902.1:n.1877+73C>A
ENST00000683513.1:c.1575+73C>A	ENSP00000506809.1:n.1575+73C>A
ENST00000263431.4:c.1575+73C>A MANE Select	ENSP00000263431.3:n.1575+73C>A
ENST00000263431.3:c.1575+73C>A	ENSP00000263431.3:n.1575+73C>A
NM_001316329.1:c.1575+73C>A	NP_001303258.1:n.1575+73C>A
NM_002739.3:c.1575+73C>A , LRG_669t1:c.1575+73C>A	NP_002730.1:n.1575+73C>A
NM_002739.4:c.1575+73C>A	NP_002730.1:n.1575+73C>A
XM_011527108.1:c.666+73C>A	XP_011525410.1:n.666+73C>A
NM_002739.5:c.1575+73C>A MANE Select	NP_002730.1:n.1575+73C>A
NM_001316329.2:c.1575+73C>A	NP_001303258.1:n.1575+73C>A