Canonical Allele Identifier: CA633905660

Gene: PRKCG

Linked Data

• dbSNP Id: rs1248868551
• gnomAD v2: 19-54403622-G-A
• gnomAD v4: 19-53900368-G-A
• MyVariant Identifiers: chr19:g.54403622G>A (hg19) ; chr19:g.53900368G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900368G>A , CM000681.2:g.53900368G>A	GRCh38
NC_000019.9:g.54403622G>A , CM000681.1:g.54403622G>A	GRCh37
NC_000019.8:g.59095434G>A	NCBI36
NG_009114.1:g.23156G>A , LRG_669:g.23156G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1373+44G>A	ENSP00000507230.1:n.1373+44G>A
ENST00000682268.1:n.1671+44G>A
ENST00000682676.1:n.774+44G>A
ENST00000682902.1:n.1675+44G>A
ENST00000683513.1:c.1373+44G>A	ENSP00000506809.1:n.1373+44G>A
ENST00000263431.4:c.1373+44G>A MANE Select	ENSP00000263431.3:n.1373+44G>A
ENST00000263431.3:c.1373+44G>A	ENSP00000263431.3:n.1373+44G>A
NM_001316329.1:c.1373+44G>A	NP_001303258.1:n.1373+44G>A
NM_002739.3:c.1373+44G>A , LRG_669t1:c.1373+44G>A	NP_002730.1:n.1373+44G>A
NM_002739.4:c.1373+44G>A	NP_002730.1:n.1373+44G>A
XM_011527108.1:c.464+44G>A	XP_011525410.1:n.464+44G>A
NM_002739.5:c.1373+44G>A MANE Select	NP_002730.1:n.1373+44G>A
NM_001316329.2:c.1373+44G>A	NP_001303258.1:n.1373+44G>A