Canonical Allele Identifier: CA16043864

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 374716
• ClinVar RCV Id: RCV000415865
• dbSNP Id: rs1057519215
• MyVariant Identifiers: chr19:g.54386419G>A (hg19) ; chr19:g.53883165G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53883165G>A , CM000681.2:g.53883165G>A	GRCh38
NC_000019.9:g.54386419G>A , CM000681.1:g.54386419G>A	GRCh37
NC_000019.8:g.59078231G>A	NCBI36
NG_009114.1:g.5953G>A , LRG_669:g.5953G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.173G>A	ENSP00000507230.1:p.Gly58Asp
ENST00000682268.1:n.471G>A
ENST00000682902.1:n.475G>A
ENST00000683513.1:c.173G>A	ENSP00000506809.1:p.Gly58Asp
ENST00000263431.4:c.173G>A MANE Select	ENSP00000263431.3:p.Gly58Asp
ENST00000263431.3:c.173G>A	ENSP00000263431.3:p.Gly58Asp
ENST00000419486.1:c.-212G>A	ENSP00000387919.2:n.-212G>A
ENST00000474397.5:c.-212G>A	ENSP00000471271.1:n.-212G>A
ENST00000479081.5:c.-212G>A	ENSP00000471544.1:n.-212G>A
NM_001316329.1:c.173G>A	NP_001303258.1:p.Gly58Asp
NM_002739.3:c.173G>A , LRG_669t1:c.173G>A	NP_002730.1:p.Gly58Asp
NM_002739.4:c.173G>A	NP_002730.1:p.Gly58Asp
NM_002739.5:c.173G>A MANE Select	NP_002730.1:p.Gly58Asp
NM_001316329.2:c.173G>A	NP_001303258.1:p.Gly58Asp