Canonical Allele Identifier: CA508788667

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53890013-A-G
• MyVariant Identifiers: chr19:g.54393267A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890013A>G , CM000681.2:g.53890013A>G	GRCh38
NC_000019.9:g.54393267A>G , CM000681.1:g.54393267A>G	GRCh37
NC_000019.8:g.59085079A>G	NCBI36
NG_009114.1:g.12801A>G , LRG_669:g.12801A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.525A>G	ENSP00000507230.1:p.Val175=
ENST00000682268.1:n.823A>G
ENST00000682902.1:n.827A>G
ENST00000683513.1:c.525A>G	ENSP00000506809.1:p.Val175=
ENST00000263431.4:c.525A>G MANE Select	ENSP00000263431.3:p.Val175=
ENST00000263431.3:c.525A>G	ENSP00000263431.3:p.Val175=
ENST00000474397.5:c.141A>G	ENSP00000471271.1:p.Val47=
NM_001316329.1:c.525A>G	NP_001303258.1:p.Val175=
NM_002739.3:c.525A>G , LRG_669t1:c.525A>G	NP_002730.1:p.Val175=
NM_002739.4:c.525A>G	NP_002730.1:p.Val175=
NM_002739.5:c.525A>G MANE Select	NP_002730.1:p.Val175=
NM_001316329.2:c.525A>G	NP_001303258.1:p.Val175=