Canonical Allele Identifier: CA2528008765
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900043_53900048dup , CM000681.2:g.53900043_53900048dup GRCh38
NC_000019.9:g.54403297_54403302dup , CM000681.1:g.54403297_54403302dup GRCh37
NC_000019.8:g.59095109_59095114dup NCBI36
NG_009114.1:g.22831_22836dup , LRG_669:g.22831_22836dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.1282-190_1282-185dup ENSP00000507230.1:n.1282-190_1282-185dup
ENST00000682268.1:n.1580-190_1580-185dup
ENST00000682676.1:n.683-190_683-185dup
ENST00000682902.1:n.1584-190_1584-185dup
ENST00000683513.1:c.1282-190_1282-185dup ENSP00000506809.1:n.1282-190_1282-185dup
ENST00000263431.4:c.1282-190_1282-185dup MANE Select ENSP00000263431.3:n.1282-190_1282-185dup
ENST00000263431.3:c.1282-190_1282-185dup ENSP00000263431.3:n.1282-190_1282-185dup
NM_001316329.1:c.1282-190_1282-185dup NP_001303258.1:n.1282-190_1282-185dup
NM_002739.3:c.1282-190_1282-185dup , LRG_669t1:c.1282-190_1282-185dup NP_002730.1:n.1282-190_1282-185dup
NM_002739.4:c.1282-190_1282-185dup NP_002730.1:n.1282-190_1282-185dup
XM_011527108.1:c.373-190_373-185dup XP_011525410.1:n.373-190_373-185dup
NM_002739.5:c.1282-190_1282-185dup MANE Select NP_002730.1:n.1282-190_1282-185dup
NM_001316329.2:c.1282-190_1282-185dup NP_001303258.1:n.1282-190_1282-185dup