Canonical Allele Identifier: CA407412166
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882631C>T , CM000681.2:g.53882631C>T GRCh38
NC_000019.9:g.54385885C>T , CM000681.1:g.54385885C>T GRCh37
NC_000019.8:g.59077697C>T NCBI36
NG_009114.1:g.5419C>T , LRG_669:g.5419C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.137C>T ENSP00000507230.1:p.Pro46Leu
ENST00000682268.1:n.435C>T
ENST00000682902.1:n.439C>T
ENST00000683513.1:c.137C>T ENSP00000506809.1:p.Pro46Leu
ENST00000263431.4:c.137C>T MANE Select ENSP00000263431.3:p.Pro46Leu
ENST00000263431.3:c.137C>T ENSP00000263431.3:p.Pro46Leu
ENST00000419486.1:c.-248C>T ENSP00000387919.2:n.-248C>T
ENST00000474397.5:c.-248C>T ENSP00000471271.1:n.-248C>T
ENST00000479081.5:c.-248C>T ENSP00000471544.1:n.-248C>T
NM_001316329.1:c.137C>T NP_001303258.1:p.Pro46Leu
NM_002739.3:c.137C>T , LRG_669t1:c.137C>T NP_002730.1:p.Pro46Leu
NM_002739.4:c.137C>T NP_002730.1:p.Pro46Leu
NM_002739.5:c.137C>T MANE Select NP_002730.1:p.Pro46Leu
NM_001316329.2:c.137C>T NP_001303258.1:p.Pro46Leu