Canonical Allele Identifier: CA2576878475

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889538T>C , CM000681.2:g.53889538T>C	GRCh38
NC_000019.9:g.54392792T>C , CM000681.1:g.54392792T>C	GRCh37
NC_000019.8:g.59084604T>C	NCBI36
NG_009114.1:g.12326T>C , LRG_669:g.12326T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.286-100T>C	ENSP00000507230.1:n.286-100T>C
ENST00000682268.1:n.584-100T>C
ENST00000682902.1:n.588-100T>C
ENST00000683513.1:c.286-100T>C	ENSP00000506809.1:n.286-100T>C
ENST00000263431.4:c.286-100T>C MANE Select	ENSP00000263431.3:n.286-100T>C
ENST00000263431.3:c.286-100T>C	ENSP00000263431.3:n.286-100T>C
ENST00000419486.1:c.-99-100T>C	ENSP00000387919.2:n.-99-100T>C
ENST00000474397.5:c.-99-100T>C	ENSP00000471271.1:n.-99-100T>C
ENST00000479081.5:c.-99-100T>C	ENSP00000471544.1:n.-99-100T>C
NM_001316329.1:c.286-100T>C	NP_001303258.1:n.286-100T>C
NM_002739.3:c.286-100T>C , LRG_669t1:c.286-100T>C	NP_002730.1:n.286-100T>C
NM_002739.4:c.286-100T>C	NP_002730.1:n.286-100T>C
NM_002739.5:c.286-100T>C MANE Select	NP_002730.1:n.286-100T>C
NM_001316329.2:c.286-100T>C	NP_001303258.1:n.286-100T>C