Canonical Allele Identifier: CA407418652

Gene: PRKCG

Linked Data

• MyVariant Identifiers: chr19:g.54403889G>A (hg19) ; chr19:g.53900635G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900635G>A , CM000681.2:g.53900635G>A	GRCh38
NC_000019.9:g.54403889G>A , CM000681.1:g.54403889G>A	GRCh37
NC_000019.8:g.59095701G>A	NCBI36
NG_009114.1:g.23423G>A , LRG_669:g.23423G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1461G>A	ENSP00000507230.1:p.Met487Ile
ENST00000682268.1:n.1759G>A
ENST00000682676.1:n.862G>A
ENST00000682902.1:n.1763G>A
ENST00000683513.1:c.1461G>A	ENSP00000506809.1:p.Met487Ile
ENST00000263431.4:c.1461G>A MANE Select	ENSP00000263431.3:p.Met487Ile
ENST00000263431.3:c.1461G>A	ENSP00000263431.3:p.Met487Ile
NM_001316329.1:c.1461G>A	NP_001303258.1:p.Met487Ile
NM_002739.3:c.1461G>A , LRG_669t1:c.1461G>A	NP_002730.1:p.Met487Ile
NM_002739.4:c.1461G>A	NP_002730.1:p.Met487Ile
XM_011527108.1:c.552G>A	XP_011525410.1:p.Met184Ile
NM_002739.5:c.1461G>A MANE Select	NP_002730.1:p.Met487Ile
NM_001316329.2:c.1461G>A	NP_001303258.1:p.Met487Ile