Canonical Allele Identifier: CA407414112
Gene: PRKCG HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.54392909C>A (hg19) chr19:g.53889655C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889655C>A , CM000681.2:g.53889655C>A GRCh38
NC_000019.9:g.54392909C>A , CM000681.1:g.54392909C>A GRCh37
NC_000019.8:g.59084721C>A NCBI36
NG_009114.1:g.12443C>A , LRG_669:g.12443C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.303C>A ENSP00000507230.1:p.His101Gln
ENST00000682268.1:n.601C>A
ENST00000682902.1:n.605C>A
ENST00000683513.1:c.303C>A ENSP00000506809.1:p.His101Gln
ENST00000263431.4:c.303C>A MANE Select ENSP00000263431.3:p.His101Gln
ENST00000263431.3:c.303C>A ENSP00000263431.3:p.His101Gln
ENST00000419486.1:c.-82C>A ENSP00000387919.2:n.-82C>A
ENST00000474397.5:c.-82C>A ENSP00000471271.1:n.-82C>A
ENST00000479081.5:c.-82C>A ENSP00000471544.1:n.-82C>A
NM_001316329.1:c.303C>A NP_001303258.1:p.His101Gln
NM_002739.3:c.303C>A , LRG_669t1:c.303C>A NP_002730.1:p.His101Gln
NM_002739.4:c.303C>A NP_002730.1:p.His101Gln
NM_002739.5:c.303C>A MANE Select NP_002730.1:p.His101Gln
NM_001316329.2:c.303C>A NP_001303258.1:p.His101Gln
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