Canonical Allele Identifier: CA508785726

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889646-G-T
• MyVariant Identifiers: chr19:g.54392900G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889646G>T , CM000681.2:g.53889646G>T	GRCh38
NC_000019.9:g.54392900G>T , CM000681.1:g.54392900G>T	GRCh37
NC_000019.8:g.59084712G>T	NCBI36
NG_009114.1:g.12434G>T , LRG_669:g.12434G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.294G>T	ENSP00000507230.1:p.Arg98=
ENST00000682268.1:n.592G>T
ENST00000682902.1:n.596G>T
ENST00000683513.1:c.294G>T	ENSP00000506809.1:p.Arg98=
ENST00000263431.4:c.294G>T MANE Select	ENSP00000263431.3:p.Arg98=
ENST00000263431.3:c.294G>T	ENSP00000263431.3:p.Arg98=
ENST00000419486.1:c.-91G>T	ENSP00000387919.2:n.-91G>T
ENST00000474397.5:c.-91G>T	ENSP00000471271.1:n.-91G>T
ENST00000479081.5:c.-91G>T	ENSP00000471544.1:n.-91G>T
NM_001316329.1:c.294G>T	NP_001303258.1:p.Arg98=
NM_002739.3:c.294G>T , LRG_669t1:c.294G>T	NP_002730.1:p.Arg98=
NM_002739.4:c.294G>T	NP_002730.1:p.Arg98=
NM_002739.5:c.294G>T MANE Select	NP_002730.1:p.Arg98=
NM_001316329.2:c.294G>T	NP_001303258.1:p.Arg98=