Canonical Allele Identifier: CA2586963392

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889941-TGTGGACCACAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889942_53889952del , CM000681.2:g.53889942_53889952del	GRCh38
NC_000019.9:g.54393196_54393206del , CM000681.1:g.54393196_54393206del	GRCh37
NC_000019.8:g.59085008_59085018del	NCBI36
NG_009114.1:g.12730_12740del , LRG_669:g.12730_12740del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.454_464del	ENSP00000507230.1:p.Val152ArgfsTer17
ENST00000682268.1:n.752_762del
ENST00000682902.1:n.756_766del
ENST00000683513.1:c.454_464del	ENSP00000506809.1:p.Val152ArgfsTer17
ENST00000263431.4:c.454_464del MANE Select	ENSP00000263431.3:p.Val152ArgfsTer17
ENST00000263431.3:c.454_464del	ENSP00000263431.3:p.Val152ArgfsTer17
ENST00000419486.1:c.70_80del	ENSP00000387919.2:p.Val24ArgfsTer?
ENST00000474397.5:c.70_80del	ENSP00000471271.1:p.Val24ArgfsTer17
NM_001316329.1:c.454_464del	NP_001303258.1:p.Val152ArgfsTer17
NM_002739.3:c.454_464del , LRG_669t1:c.454_464del	NP_002730.1:p.Val152ArgfsTer17
NM_002739.4:c.454_464del	NP_002730.1:p.Val152ArgfsTer17
NM_002739.5:c.454_464del MANE Select	NP_002730.1:p.Val152ArgfsTer17
NM_001316329.2:c.454_464del	NP_001303258.1:p.Val152ArgfsTer17