Canonical Allele Identifier: CA407414526

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889974-G-T
• MyVariant Identifiers: chr19:g.54393228G>T (hg19) ; chr19:g.53889974G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889974G>T , CM000681.2:g.53889974G>T	GRCh38
NC_000019.9:g.54393228G>T , CM000681.1:g.54393228G>T	GRCh37
NC_000019.8:g.59085040G>T	NCBI36
NG_009114.1:g.12762G>T , LRG_669:g.12762G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.486G>T	ENSP00000507230.1:p.Gln162His
ENST00000682268.1:n.784G>T
ENST00000682902.1:n.788G>T
ENST00000683513.1:c.486G>T	ENSP00000506809.1:p.Gln162His
ENST00000263431.4:c.486G>T MANE Select	ENSP00000263431.3:p.Gln162His
ENST00000263431.3:c.486G>T	ENSP00000263431.3:p.Gln162His
ENST00000419486.1:c.102G>T	ENSP00000387919.2:p.Gln34His
ENST00000474397.5:c.102G>T	ENSP00000471271.1:p.Gln34His
NM_001316329.1:c.486G>T	NP_001303258.1:p.Gln162His
NM_002739.3:c.486G>T , LRG_669t1:c.486G>T	NP_002730.1:p.Gln162His
NM_002739.4:c.486G>T	NP_002730.1:p.Gln162His
NM_002739.5:c.486G>T MANE Select	NP_002730.1:p.Gln162His
NM_001316329.2:c.486G>T	NP_001303258.1:p.Gln162His