Canonical Allele Identifier: CA2342579249

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889647_53889653delinsAACAAAC , CM000681.2:g.53889647_53889653delinsAACAAAC	GRCh38
NC_000019.9:g.54392901_54392907delinsAACAAAC , CM000681.1:g.54392901_54392907delinsAACAAAC	GRCh37
NC_000019.8:g.59084713_59084719delinsAACAAAC	NCBI36
NG_009114.1:g.12435_12441delinsAACAAAC , LRG_669:g.12435_12441delinsAACAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.295_301delinsAACAAAC	ENSP00000507230.1:p.Asn99=
ENST00000682268.1:n.593_599delinsAACAAAC
ENST00000682902.1:n.597_603delinsAACAAAC
ENST00000683513.1:c.295_301delinsAACAAAC	ENSP00000506809.1:p.Asn99=
ENST00000263431.4:c.295_301delinsAACAAAC MANE Select	ENSP00000263431.3:p.Asn99=
ENST00000263431.3:c.295_301delinsAACAAAC	ENSP00000263431.3:p.Asn99=
ENST00000419486.1:c.-90_-84delinsAACAAAC	ENSP00000387919.2:n.-90_-84delinsAACAAAC
ENST00000474397.5:c.-90_-84delinsAACAAAC	ENSP00000471271.1:n.-90_-84delinsAACAAAC
ENST00000479081.5:c.-90_-84delinsAACAAAC	ENSP00000471544.1:n.-90_-84delinsAACAAAC
NM_001316329.1:c.295_301delinsAACAAAC	NP_001303258.1:p.Asn99=
NM_002739.3:c.295_301delinsAACAAAC , LRG_669t1:c.295_301delinsAACAAAC	NP_002730.1:p.Asn99=
NM_002739.4:c.295_301delinsAACAAAC	NP_002730.1:p.Asn99=
NM_002739.5:c.295_301delinsAACAAAC MANE Select	NP_002730.1:p.Asn99=
NM_001316329.2:c.295_301delinsAACAAAC	NP_001303258.1:p.Asn99=