Canonical Allele Identifier: CA2586962389
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882295_53882321dup , CM000681.2:g.53882295_53882321dup GRCh38
NC_000019.9:g.54385549_54385575dup , CM000681.1:g.54385549_54385575dup GRCh37
NC_000019.8:g.59077361_59077387dup NCBI36
NG_009114.1:g.5083_5109dup , LRG_669:g.5083_5109dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-200_-174dup ENSP00000507230.1:n.-200_-174dup
ENST00000682268.1:n.99_125dup
ENST00000682902.1:n.103_129dup
ENST00000683513.1:c.-200_-174dup ENSP00000506809.1:n.-200_-174dup
ENST00000263431.4:c.-200_-174dup MANE Select ENSP00000263431.3:n.-200_-174dup
ENST00000263431.3:c.-200_-174dup ENSP00000263431.3:n.-200_-174dup
ENST00000419486.1:c.-387_-361dup ENSP00000387919.2:n.-387_-361dup
ENST00000474397.5:c.-322-262_-322-236dup ENSP00000471271.1:n.-322-262_-322-236dup
ENST00000479081.5:c.-322-262_-322-236dup ENSP00000471544.1:n.-322-262_-322-236dup
NM_001316329.1:c.-200_-174dup NP_001303258.1:n.-200_-174dup
NM_002739.3:c.-200_-174dup , LRG_669t1:c.-200_-174dup NP_002730.1:n.-200_-174dup
NM_002739.4:c.-200_-174dup NP_002730.1:n.-200_-174dup
NM_002739.5:c.-200_-174dup MANE Select NP_002730.1:n.-200_-174dup
NM_001316329.2:c.-200_-174dup NP_001303258.1:n.-200_-174dup