Canonical Allele Identifier: CA407418629

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 2585226
• ClinVar RCV Id: RCV003337842
• MyVariant Identifiers: chr19:g.54403879A>T (hg19) ; chr19:g.53900625A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900625A>T , CM000681.2:g.53900625A>T	GRCh38
NC_000019.9:g.54403879A>T , CM000681.1:g.54403879A>T	GRCh37
NC_000019.8:g.59095691A>T	NCBI36
NG_009114.1:g.23413A>T , LRG_669:g.23413A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1451A>T	ENSP00000507230.1:p.Asp484Val
ENST00000682268.1:n.1749A>T
ENST00000682676.1:n.852A>T
ENST00000682902.1:n.1753A>T
ENST00000683513.1:c.1451A>T	ENSP00000506809.1:p.Asp484Val
ENST00000263431.4:c.1451A>T MANE Select	ENSP00000263431.3:p.Asp484Val
ENST00000263431.3:c.1451A>T	ENSP00000263431.3:p.Asp484Val
NM_001316329.1:c.1451A>T	NP_001303258.1:p.Asp484Val
NM_002739.3:c.1451A>T , LRG_669t1:c.1451A>T	NP_002730.1:p.Asp484Val
NM_002739.4:c.1451A>T	NP_002730.1:p.Asp484Val
XM_011527108.1:c.542A>T	XP_011525410.1:p.Asp181Val
NM_002739.5:c.1451A>T MANE Select	NP_002730.1:p.Asp484Val
NM_001316329.2:c.1451A>T	NP_001303258.1:p.Asp484Val