Canonical Allele Identifier: CA2342575762
Gene: PRKCG HGNC NCBI

Linked Data

dbSNP Id: rs1159681689

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882238_53882240dup , CM000681.2:g.53882238_53882240dup GRCh38
NC_000019.9:g.54385492_54385494dup , CM000681.1:g.54385492_54385494dup GRCh37
NC_000019.8:g.59077304_59077306dup NCBI36
NG_009114.1:g.5026_5028dup , LRG_669:g.5026_5028dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-257_-255dup ENSP00000507230.1:n.-257_-255dup
ENST00000682268.1:n.42_44dup
ENST00000682902.1:n.46_48dup
ENST00000683513.1:c.-257_-255dup ENSP00000506809.1:n.-257_-255dup
ENST00000263431.4:c.-257_-255dup MANE Select ENSP00000263431.3:n.-257_-255dup
ENST00000263431.3:c.-257_-255dup ENSP00000263431.3:n.-257_-255dup
ENST00000419486.1:c.-444_-442dup ENSP00000387919.2:n.-444_-442dup
ENST00000474397.5:c.-322-319_-322-317dup ENSP00000471271.1:n.-322-319_-322-317dup
ENST00000479081.5:c.-322-319_-322-317dup ENSP00000471544.1:n.-322-319_-322-317dup
NM_001316329.1:c.-257_-255dup NP_001303258.1:n.-257_-255dup
NM_002739.3:c.-257_-255dup , LRG_669t1:c.-257_-255dup NP_002730.1:n.-257_-255dup
NM_002739.4:c.-257_-255dup NP_002730.1:n.-257_-255dup
NM_002739.5:c.-257_-255dup MANE Select NP_002730.1:n.-257_-255dup
NM_001316329.2:c.-257_-255dup NP_001303258.1:n.-257_-255dup