Canonical Allele Identifier: CA2342579394

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889937_53889938delinsGC , CM000681.2:g.53889937_53889938delinsGC	GRCh38
NC_000019.9:g.54393191_54393192delinsGC , CM000681.1:g.54393191_54393192delinsGC	GRCh37
NC_000019.8:g.59085003_59085004delinsGC	NCBI36
NG_009114.1:g.12725_12726delinsGC , LRG_669:g.12725_12726delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.449_450delinsGC	ENSP00000507230.1:p.Cys150=
ENST00000682268.1:n.747_748delinsGC
ENST00000682902.1:n.751_752delinsGC
ENST00000683513.1:c.449_450delinsGC	ENSP00000506809.1:p.Cys150=
ENST00000263431.4:c.449_450delinsGC MANE Select	ENSP00000263431.3:p.Cys150=
ENST00000263431.3:c.449_450delinsGC	ENSP00000263431.3:p.Cys150=
ENST00000419486.1:c.65_66delinsGC	ENSP00000387919.2:p.Cys22=
ENST00000474397.5:c.65_66delinsGC	ENSP00000471271.1:p.Cys22=
NM_001316329.1:c.449_450delinsGC	NP_001303258.1:p.Cys150=
NM_002739.3:c.449_450delinsGC , LRG_669t1:c.449_450delinsGC	NP_002730.1:p.Cys150=
NM_002739.4:c.449_450delinsGC	NP_002730.1:p.Cys150=
NM_002739.5:c.449_450delinsGC MANE Select	NP_002730.1:p.Cys150=
NM_001316329.2:c.449_450delinsGC	NP_001303258.1:p.Cys150=