Canonical Allele Identifier: CA407414620

Gene: PRKCG

Linked Data

• MyVariant Identifiers: chr19:g.54393273T>G (hg19) ; chr19:g.53890019T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890019T>G , CM000681.2:g.53890019T>G	GRCh38
NC_000019.9:g.54393273T>G , CM000681.1:g.54393273T>G	GRCh37
NC_000019.8:g.59085085T>G	NCBI36
NG_009114.1:g.12807T>G , LRG_669:g.12807T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+2T>G	ENSP00000507230.1:n.529+2T>G
ENST00000682268.1:n.827+2T>G
ENST00000682902.1:n.831+2T>G
ENST00000683513.1:c.529+2T>G	ENSP00000506809.1:n.529+2T>G
ENST00000263431.4:c.529+2T>G MANE Select	ENSP00000263431.3:n.529+2T>G
ENST00000263431.3:c.529+2T>G	ENSP00000263431.3:n.529+2T>G
ENST00000474397.5:c.145+2T>G	ENSP00000471271.1:n.145+2T>G
NM_001316329.1:c.529+2T>G	NP_001303258.1:n.529+2T>G
NM_002739.3:c.529+2T>G , LRG_669t1:c.529+2T>G	NP_002730.1:n.529+2T>G
NM_002739.4:c.529+2T>G	NP_002730.1:n.529+2T>G
NM_002739.5:c.529+2T>G MANE Select	NP_002730.1:n.529+2T>G
NM_001316329.2:c.529+2T>G	NP_001303258.1:n.529+2T>G