Canonical Allele Identifier: CA310092099

Gene: PRKCG

Linked Data

• dbSNP Id: rs35629728
• MyVariant Identifiers: chr19:g.54403650_54403651insC (hg19) ; chr19:g.53900396_53900397insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900400dup , CM000681.2:g.53900400dup	GRCh38
NC_000019.9:g.54403654dup , CM000681.1:g.54403654dup	GRCh37
NC_000019.8:g.59095466dup	NCBI36
NG_009114.1:g.23188dup , LRG_669:g.23188dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1374-19dup	ENSP00000507230.1:n.1374-19dup
ENST00000682268.1:n.1672-19dup
ENST00000682676.1:n.775-19dup
ENST00000682902.1:n.1676-19dup
ENST00000683513.1:c.1374-19dup	ENSP00000506809.1:n.1374-19dup
ENST00000263431.4:c.1374-19dup MANE Select	ENSP00000263431.3:n.1374-19dup
ENST00000263431.3:c.1374-19dup	ENSP00000263431.3:n.1374-19dup
NM_001316329.1:c.1374-19dup	NP_001303258.1:n.1374-19dup
NM_002739.3:c.1374-19dup , LRG_669t1:c.1374-19dup	NP_002730.1:n.1374-19dup
NM_002739.4:c.1374-19dup	NP_002730.1:n.1374-19dup
XM_011527108.1:c.465-19dup	XP_011525410.1:n.465-19dup
NM_002739.5:c.1374-19dup MANE Select	NP_002730.1:n.1374-19dup
NM_001316329.2:c.1374-19dup	NP_001303258.1:n.1374-19dup