Canonical Allele Identifier: CA508795071

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900250-G-T
• MyVariant Identifiers: chr19:g.54403504G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900250G>T , CM000681.2:g.53900250G>T	GRCh38
NC_000019.9:g.54403504G>T , CM000681.1:g.54403504G>T	GRCh37
NC_000019.8:g.59095316G>T	NCBI36
NG_009114.1:g.23038G>T , LRG_669:g.23038G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1299G>T	ENSP00000507230.1:p.Val433=
ENST00000682268.1:n.1597G>T
ENST00000682676.1:n.700G>T
ENST00000682902.1:n.1601G>T
ENST00000683513.1:c.1299G>T	ENSP00000506809.1:p.Val433=
ENST00000263431.4:c.1299G>T MANE Select	ENSP00000263431.3:p.Val433=
ENST00000263431.3:c.1299G>T	ENSP00000263431.3:p.Val433=
NM_001316329.1:c.1299G>T	NP_001303258.1:p.Val433=
NM_002739.3:c.1299G>T , LRG_669t1:c.1299G>T	NP_002730.1:p.Val433=
NM_002739.4:c.1299G>T	NP_002730.1:p.Val433=
XM_011527108.1:c.390G>T	XP_011525410.1:p.Val130=
NM_002739.5:c.1299G>T MANE Select	NP_002730.1:p.Val433=
NM_001316329.2:c.1299G>T	NP_001303258.1:p.Val433=