Canonical Allele Identifier: CA2586962583

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53882535-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882535_53882536insC , CM000681.2:g.53882535_53882536insC	GRCh38
NC_000019.9:g.54385789_54385790insC , CM000681.1:g.54385789_54385790insC	GRCh37
NC_000019.8:g.59077601_59077602insC	NCBI36
NG_009114.1:g.5323_5324insC , LRG_669:g.5323_5324insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.41_42insC	ENSP00000507230.1:p.Pro15ThrfsTer?
ENST00000682268.1:n.339_340insC
ENST00000682902.1:n.343_344insC
ENST00000683513.1:c.41_42insC	ENSP00000506809.1:p.Pro15ThrfsTer?
ENST00000263431.4:c.41_42insC MANE Select	ENSP00000263431.3:p.Pro15ThrfsTer?
ENST00000263431.3:c.41_42insC	ENSP00000263431.3:p.Pro15ThrfsTer?
ENST00000419486.1:c.-322-22_-322-21insC	ENSP00000387919.2:n.-322-22_-322-21insC
ENST00000474397.5:c.-322-22_-322-21insC	ENSP00000471271.1:n.-322-22_-322-21insC
ENST00000479081.5:c.-322-22_-322-21insC	ENSP00000471544.1:n.-322-22_-322-21insC
NM_001316329.1:c.41_42insC	NP_001303258.1:p.Pro15ThrfsTer?
NM_002739.3:c.41_42insC , LRG_669t1:c.41_42insC	NP_002730.1:p.Pro15ThrfsTer?
NM_002739.4:c.41_42insC	NP_002730.1:p.Pro15ThrfsTer?
NM_002739.5:c.41_42insC MANE Select	NP_002730.1:p.Pro15ThrfsTer?
NM_001316329.2:c.41_42insC	NP_001303258.1:p.Pro15ThrfsTer?