Canonical Allele Identifier: CA2342584759
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900564A= , CM000681.2:g.53900564A= GRCh38
NC_000019.9:g.54403818A= , CM000681.1:g.54403818A= GRCh37
NC_000019.8:g.59095630A= NCBI36
NG_009114.1:g.23352A= , LRG_669:g.23352A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.1437-47A= ENSP00000507230.1:n.1437-47A=
ENST00000682268.1:n.1735-47A=
ENST00000682676.1:n.838-47A=
ENST00000682902.1:n.1739-47A=
ENST00000683513.1:c.1437-47A= ENSP00000506809.1:n.1437-47A=
ENST00000263431.4:c.1437-47A= MANE Select ENSP00000263431.3:n.1437-47A=
ENST00000263431.3:c.1437-47A= ENSP00000263431.3:n.1437-47A=
NM_001316329.1:c.1437-47A= NP_001303258.1:n.1437-47A=
NM_002739.3:c.1437-47A= , LRG_669t1:c.1437-47A= NP_002730.1:n.1437-47A=
NM_002739.4:c.1437-47A= NP_002730.1:n.1437-47A=
XM_011527108.1:c.528-47A= XP_011525410.1:n.528-47A=
NM_002739.5:c.1437-47A= MANE Select NP_002730.1:n.1437-47A=
NM_001316329.2:c.1437-47A= NP_001303258.1:n.1437-47A=