Canonical Allele Identifier: CA508796395

Gene: PRKCG

Linked Data

• MyVariant Identifiers: chr19:g.54403919T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900665T>G , CM000681.2:g.53900665T>G	GRCh38
NC_000019.9:g.54403919T>G , CM000681.1:g.54403919T>G	GRCh37
NC_000019.8:g.59095731T>G	NCBI36
NG_009114.1:g.23453T>G , LRG_669:g.23453T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1491T>G	ENSP00000507230.1:p.Thr497=
ENST00000682268.1:n.1789T>G
ENST00000682676.1:n.892T>G
ENST00000682902.1:n.1793T>G
ENST00000683513.1:c.1491T>G	ENSP00000506809.1:p.Thr497=
ENST00000263431.4:c.1491T>G MANE Select	ENSP00000263431.3:p.Thr497=
ENST00000263431.3:c.1491T>G	ENSP00000263431.3:p.Thr497=
NM_001316329.1:c.1491T>G	NP_001303258.1:p.Thr497=
NM_002739.3:c.1491T>G , LRG_669t1:c.1491T>G	NP_002730.1:p.Thr497=
NM_002739.4:c.1491T>G	NP_002730.1:p.Thr497=
XM_011527108.1:c.582T>G	XP_011525410.1:p.Thr194=
NM_002739.5:c.1491T>G MANE Select	NP_002730.1:p.Thr497=
NM_001316329.2:c.1491T>G	NP_001303258.1:p.Thr497=