Canonical Allele Identifier: CA2576907864

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900578G>C , CM000681.2:g.53900578G>C	GRCh38
NC_000019.9:g.54403832G>C , CM000681.1:g.54403832G>C	GRCh37
NC_000019.8:g.59095644G>C	NCBI36
NG_009114.1:g.23366G>C , LRG_669:g.23366G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.1437-33G>C	ENSP00000507230.1:n.1437-33G>C
ENST00000682268.1:n.1735-33G>C
ENST00000682676.1:n.838-33G>C
ENST00000682902.1:n.1739-33G>C
ENST00000683513.1:c.1437-33G>C	ENSP00000506809.1:n.1437-33G>C
ENST00000263431.4:c.1437-33G>C MANE Select	ENSP00000263431.3:n.1437-33G>C
ENST00000263431.3:c.1437-33G>C	ENSP00000263431.3:n.1437-33G>C
NM_001316329.1:c.1437-33G>C	NP_001303258.1:n.1437-33G>C
NM_002739.3:c.1437-33G>C , LRG_669t1:c.1437-33G>C	NP_002730.1:n.1437-33G>C
NM_002739.4:c.1437-33G>C	NP_002730.1:n.1437-33G>C
XM_011527108.1:c.528-33G>C	XP_011525410.1:n.528-33G>C
NM_002739.5:c.1437-33G>C MANE Select	NP_002730.1:n.1437-33G>C
NM_001316329.2:c.1437-33G>C	NP_001303258.1:n.1437-33G>C