Canonical Allele Identifier: CA2586962582

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53882527-AGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882529_53882531del , CM000681.2:g.53882529_53882531del	GRCh38
NC_000019.9:g.54385783_54385785del , CM000681.1:g.54385783_54385785del	GRCh37
NC_000019.8:g.59077595_59077597del	NCBI36
NG_009114.1:g.5317_5319del , LRG_669:g.5317_5319del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.35_37del	ENSP00000507230.1:p.Glu12del
ENST00000682268.1:n.333_335del
ENST00000682902.1:n.337_339del
ENST00000683513.1:c.35_37del	ENSP00000506809.1:p.Glu12del
ENST00000263431.4:c.35_37del MANE Select	ENSP00000263431.3:p.Glu12del
ENST00000263431.3:c.35_37del	ENSP00000263431.3:p.Glu12del
ENST00000419486.1:c.-322-28_-322-26del	ENSP00000387919.2:n.-322-28_-322-26del
ENST00000474397.5:c.-322-28_-322-26del	ENSP00000471271.1:n.-322-28_-322-26del
ENST00000479081.5:c.-322-28_-322-26del	ENSP00000471544.1:n.-322-28_-322-26del
NM_001316329.1:c.35_37del	NP_001303258.1:p.Glu12del
NM_002739.3:c.35_37del , LRG_669t1:c.35_37del	NP_002730.1:p.Glu12del
NM_002739.4:c.35_37del	NP_002730.1:p.Glu12del
NM_002739.5:c.35_37del MANE Select	NP_002730.1:p.Glu12del
NM_001316329.2:c.35_37del	NP_001303258.1:p.Glu12del