Canonical Allele Identifier: CA407418853

Gene: PRKCG

Linked Data

• dbSNP Id: rs1336500466
• gnomAD v2: 19-54403962-A-G
• gnomAD v4: 19-53900708-A-G
• MyVariant Identifiers: chr19:g.54403962A>G (hg19) ; chr19:g.53900708A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900708A>G , CM000681.2:g.53900708A>G	GRCh38
NC_000019.9:g.54403962A>G , CM000681.1:g.54403962A>G	GRCh37
NC_000019.8:g.59095774A>G	NCBI36
NG_009114.1:g.23496A>G , LRG_669:g.23496A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1534A>G	ENSP00000507230.1:p.Thr512Ala
ENST00000682268.1:n.1832A>G
ENST00000682676.1:n.935A>G
ENST00000682902.1:n.1836A>G
ENST00000683513.1:c.1534A>G	ENSP00000506809.1:p.Thr512Ala
ENST00000263431.4:c.1534A>G MANE Select	ENSP00000263431.3:p.Thr512Ala
ENST00000263431.3:c.1534A>G	ENSP00000263431.3:p.Thr512Ala
NM_001316329.1:c.1534A>G	NP_001303258.1:p.Thr512Ala
NM_002739.3:c.1534A>G , LRG_669t1:c.1534A>G	NP_002730.1:p.Thr512Ala
NM_002739.4:c.1534A>G	NP_002730.1:p.Thr512Ala
XM_011527108.1:c.625A>G	XP_011525410.1:p.Thr209Ala
NM_002739.5:c.1534A>G MANE Select	NP_002730.1:p.Thr512Ala
NM_001316329.2:c.1534A>G	NP_001303258.1:p.Thr512Ala