Canonical Allele Identifier: CA2342579426

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889998A= , CM000681.2:g.53889998A=	GRCh38
NC_000019.9:g.54393252A= , CM000681.1:g.54393252A=	GRCh37
NC_000019.8:g.59085064A=	NCBI36
NG_009114.1:g.12786A= , LRG_669:g.12786A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.510A=	ENSP00000507230.1:p.Ala170=
ENST00000682268.1:n.808A=
ENST00000682902.1:n.812A=
ENST00000683513.1:c.510A=	ENSP00000506809.1:p.Ala170=
ENST00000263431.4:c.510A= MANE Select	ENSP00000263431.3:p.Ala170=
ENST00000263431.3:c.510A=	ENSP00000263431.3:p.Ala170=
ENST00000474397.5:c.126A=	ENSP00000471271.1:p.Ala42=
NM_001316329.1:c.510A=	NP_001303258.1:p.Ala170=
NM_002739.3:c.510A= , LRG_669t1:c.510A=	NP_002730.1:p.Ala170=
NM_002739.4:c.510A=	NP_002730.1:p.Ala170=
NM_002739.5:c.510A= MANE Select	NP_002730.1:p.Ala170=
NM_001316329.2:c.510A=	NP_001303258.1:p.Ala170=