Canonical Allele Identifier: CA407418672

Gene: PRKCG

Linked Data

• MyVariant Identifiers: chr19:g.54403897C>T (hg19) ; chr19:g.53900643C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900643C>T , CM000681.2:g.53900643C>T	GRCh38
NC_000019.9:g.54403897C>T , CM000681.1:g.54403897C>T	GRCh37
NC_000019.8:g.59095709C>T	NCBI36
NG_009114.1:g.23431C>T , LRG_669:g.23431C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1469C>T	ENSP00000507230.1:p.Ala490Val
ENST00000682268.1:n.1767C>T
ENST00000682676.1:n.870C>T
ENST00000682902.1:n.1771C>T
ENST00000683513.1:c.1469C>T	ENSP00000506809.1:p.Ala490Val
ENST00000263431.4:c.1469C>T MANE Select	ENSP00000263431.3:p.Ala490Val
ENST00000263431.3:c.1469C>T	ENSP00000263431.3:p.Ala490Val
NM_001316329.1:c.1469C>T	NP_001303258.1:p.Ala490Val
NM_002739.3:c.1469C>T , LRG_669t1:c.1469C>T	NP_002730.1:p.Ala490Val
NM_002739.4:c.1469C>T	NP_002730.1:p.Ala490Val
XM_011527108.1:c.560C>T	XP_011525410.1:p.Ala187Val
NM_002739.5:c.1469C>T MANE Select	NP_002730.1:p.Ala490Val
NM_001316329.2:c.1469C>T	NP_001303258.1:p.Ala490Val