Canonical Allele Identifier: CA407418348

Gene: PRKCG

Linked Data

• MyVariant Identifiers: chr19:g.54403542T>G (hg19) ; chr19:g.53900288T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900288T>G , CM000681.2:g.53900288T>G	GRCh38
NC_000019.9:g.54403542T>G , CM000681.1:g.54403542T>G	GRCh37
NC_000019.8:g.59095354T>G	NCBI36
NG_009114.1:g.23076T>G , LRG_669:g.23076T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1337T>G	ENSP00000507230.1:p.Ile446Ser
ENST00000682268.1:n.1635T>G
ENST00000682676.1:n.738T>G
ENST00000682902.1:n.1639T>G
ENST00000683513.1:c.1337T>G	ENSP00000506809.1:p.Ile446Ser
ENST00000263431.4:c.1337T>G MANE Select	ENSP00000263431.3:p.Ile446Ser
ENST00000263431.3:c.1337T>G	ENSP00000263431.3:p.Ile446Ser
NM_001316329.1:c.1337T>G	NP_001303258.1:p.Ile446Ser
NM_002739.3:c.1337T>G , LRG_669t1:c.1337T>G	NP_002730.1:p.Ile446Ser
NM_002739.4:c.1337T>G	NP_002730.1:p.Ile446Ser
XM_011527108.1:c.428T>G	XP_011525410.1:p.Ile143Ser
NM_002739.5:c.1337T>G MANE Select	NP_002730.1:p.Ile446Ser
NM_001316329.2:c.1337T>G	NP_001303258.1:p.Ile446Ser