Canonical Allele Identifier: CA2695229061

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882637_53882639del , CM000681.2:g.53882637_53882639del	GRCh38
NC_000019.9:g.54385891_54385893del , CM000681.1:g.54385891_54385893del	GRCh37
NC_000019.8:g.59077703_59077705del	NCBI36
NG_009114.1:g.5425_5427del , LRG_669:g.5425_5427del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.143_145del	ENSP00000507230.1:p.Phe48del
ENST00000682268.1:n.441_443del
ENST00000682902.1:n.445_447del
ENST00000683513.1:c.143_145del	ENSP00000506809.1:p.Phe48del
ENST00000263431.4:c.143_145del MANE Select	ENSP00000263431.3:p.Phe48del
ENST00000263431.3:c.143_145del	ENSP00000263431.3:p.Phe48del
ENST00000419486.1:c.-242_-240del	ENSP00000387919.2:n.-242_-240del
ENST00000474397.5:c.-242_-240del	ENSP00000471271.1:n.-242_-240del
ENST00000479081.5:c.-242_-240del	ENSP00000471544.1:n.-242_-240del
NM_001316329.1:c.143_145del	NP_001303258.1:p.Phe48del
NM_002739.3:c.143_145del , LRG_669t1:c.143_145del	NP_002730.1:p.Phe48del
NM_002739.4:c.143_145del	NP_002730.1:p.Phe48del
NM_002739.5:c.143_145del MANE Select	NP_002730.1:p.Phe48del
NM_001316329.2:c.143_145del	NP_001303258.1:p.Phe48del