Canonical Allele Identifier: CA407411878
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882565C>T , CM000681.2:g.53882565C>T GRCh38
NC_000019.9:g.54385819C>T , CM000681.1:g.54385819C>T GRCh37
NC_000019.8:g.59077631C>T NCBI36
NG_009114.1:g.5353C>T , LRG_669:g.5353C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.71C>T ENSP00000507230.1:p.Ala24Val
ENST00000682268.1:n.369C>T
ENST00000682902.1:n.373C>T
ENST00000683513.1:c.71C>T ENSP00000506809.1:p.Ala24Val
ENST00000263431.4:c.71C>T MANE Select ENSP00000263431.3:p.Ala24Val
ENST00000263431.3:c.71C>T ENSP00000263431.3:p.Ala24Val
ENST00000419486.1:c.-314C>T ENSP00000387919.2:n.-314C>T
ENST00000474397.5:c.-314C>T ENSP00000471271.1:n.-314C>T
ENST00000479081.5:c.-314C>T ENSP00000471544.1:n.-314C>T
NM_001316329.1:c.71C>T NP_001303258.1:p.Ala24Val
NM_002739.3:c.71C>T , LRG_669t1:c.71C>T NP_002730.1:p.Ala24Val
NM_002739.4:c.71C>T NP_002730.1:p.Ala24Val
NM_002739.5:c.71C>T MANE Select NP_002730.1:p.Ala24Val
NM_001316329.2:c.71C>T NP_001303258.1:p.Ala24Val