Canonical Allele Identifier: CA2739629905

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882313G>T , CM000681.2:g.53882313G>T	GRCh38
NC_000019.9:g.54385567G>T , CM000681.1:g.54385567G>T	GRCh37
NC_000019.8:g.59077379G>T	NCBI36
NG_009114.1:g.5101G>T , LRG_669:g.5101G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-182G>T	ENSP00000507230.1:n.-182G>T
ENST00000682268.1:n.117G>T
ENST00000682902.1:n.121G>T
ENST00000683513.1:c.-182G>T	ENSP00000506809.1:n.-182G>T
ENST00000263431.4:c.-182G>T MANE Select	ENSP00000263431.3:n.-182G>T
ENST00000263431.3:c.-182G>T	ENSP00000263431.3:n.-182G>T
ENST00000419486.1:c.-369G>T	ENSP00000387919.2:n.-369G>T
ENST00000474397.5:c.-322-244G>T	ENSP00000471271.1:n.-322-244G>T
ENST00000479081.5:c.-322-244G>T	ENSP00000471544.1:n.-322-244G>T
NM_001316329.1:c.-182G>T	NP_001303258.1:n.-182G>T
NM_002739.3:c.-182G>T , LRG_669t1:c.-182G>T	NP_002730.1:n.-182G>T
NM_002739.4:c.-182G>T	NP_002730.1:n.-182G>T
NM_002739.5:c.-182G>T MANE Select	NP_002730.1:n.-182G>T
NM_001316329.2:c.-182G>T	NP_001303258.1:n.-182G>T