Canonical Allele Identifier: CA2586963395

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889952-CCGAGCGCCGCGGGCGCCTGCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889953_53889973del , CM000681.2:g.53889953_53889973del	GRCh38
NC_000019.9:g.54393207_54393227del , CM000681.1:g.54393207_54393227del	GRCh37
NC_000019.8:g.59085019_59085039del	NCBI36
NG_009114.1:g.12741_12761del , LRG_669:g.12741_12761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.465_485del	ENSP00000507230.1:p.Glu156_Gln162del
ENST00000682268.1:n.763_783del
ENST00000682902.1:n.767_787del
ENST00000683513.1:c.465_485del	ENSP00000506809.1:p.Glu156_Gln162del
ENST00000263431.4:c.465_485del MANE Select	ENSP00000263431.3:p.Glu156_Gln162del
ENST00000263431.3:c.465_485del	ENSP00000263431.3:p.Glu156_Gln162del
ENST00000419486.1:c.81_101del	ENSP00000387919.2:p.Glu28_Gln34del
ENST00000474397.5:c.81_101del	ENSP00000471271.1:p.Glu28_Gln34del
NM_001316329.1:c.465_485del	NP_001303258.1:p.Glu156_Gln162del
NM_002739.3:c.465_485del , LRG_669t1:c.465_485del	NP_002730.1:p.Glu156_Gln162del
NM_002739.4:c.465_485del	NP_002730.1:p.Glu156_Gln162del
NM_002739.5:c.465_485del MANE Select	NP_002730.1:p.Glu156_Gln162del
NM_001316329.2:c.465_485del	NP_001303258.1:p.Glu156_Gln162del