Canonical Allele Identifier: CA2342584894

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900917A= , CM000681.2:g.53900917A=	GRCh38
NC_000019.9:g.54404171A= , CM000681.1:g.54404171A=	GRCh37
NC_000019.8:g.59095983A=	NCBI36
NG_009114.1:g.23705A= , LRG_669:g.23705A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+168A=	ENSP00000507230.1:n.1575+168A=
ENST00000682268.1:n.1873+168A=
ENST00000682676.1:n.976+168A=
ENST00000682902.1:n.1877+168A=
ENST00000683513.1:c.1575+168A=	ENSP00000506809.1:n.1575+168A=
ENST00000263431.4:c.1575+168A= MANE Select	ENSP00000263431.3:n.1575+168A=
ENST00000263431.3:c.1575+168A=	ENSP00000263431.3:n.1575+168A=
NM_001316329.1:c.1575+168A=	NP_001303258.1:n.1575+168A=
NM_002739.3:c.1575+168A= , LRG_669t1:c.1575+168A=	NP_002730.1:n.1575+168A=
NM_002739.4:c.1575+168A=	NP_002730.1:n.1575+168A=
XM_011527108.1:c.666+168A=	XP_011525410.1:n.666+168A=
NM_002739.5:c.1575+168A= MANE Select	NP_002730.1:n.1575+168A=
NM_001316329.2:c.1575+168A=	NP_001303258.1:n.1575+168A=