Canonical Allele Identifier: CA407418641

Gene: PRKCG

Linked Data

• MyVariant Identifiers: chr19:g.54403884G>C (hg19) ; chr19:g.53900630G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900630G>C , CM000681.2:g.53900630G>C	GRCh38
NC_000019.9:g.54403884G>C , CM000681.1:g.54403884G>C	GRCh37
NC_000019.8:g.59095696G>C	NCBI36
NG_009114.1:g.23418G>C , LRG_669:g.23418G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1456G>C	ENSP00000507230.1:p.Val486Leu
ENST00000682268.1:n.1754G>C
ENST00000682676.1:n.857G>C
ENST00000682902.1:n.1758G>C
ENST00000683513.1:c.1456G>C	ENSP00000506809.1:p.Val486Leu
ENST00000263431.4:c.1456G>C MANE Select	ENSP00000263431.3:p.Val486Leu
ENST00000263431.3:c.1456G>C	ENSP00000263431.3:p.Val486Leu
NM_001316329.1:c.1456G>C	NP_001303258.1:p.Val486Leu
NM_002739.3:c.1456G>C , LRG_669t1:c.1456G>C	NP_002730.1:p.Val486Leu
NM_002739.4:c.1456G>C	NP_002730.1:p.Val486Leu
XM_011527108.1:c.547G>C	XP_011525410.1:p.Val183Leu
NM_002739.5:c.1456G>C MANE Select	NP_002730.1:p.Val486Leu
NM_001316329.2:c.1456G>C	NP_001303258.1:p.Val486Leu