Canonical Allele Identifier: CA2830535932
Gene: PRKCI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170275469C>T , CM000665.2:g.170275469C>T GRCh38
NC_000003.11:g.169993257C>T , CM000665.1:g.169993257C>T GRCh37
NC_000003.10:g.171475951C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295797.5:c.705+182C>T MANE Select ENSP00000295797.4:n.705+182C>T
ENST00000295797.4:c.705+182C>T ENSP00000295797.4:n.705+182C>T
NM_002740.5:c.705+182C>T NP_002731.4:n.705+182C>T
XM_017006860.1:c.309+182C>T XP_016862349.1:n.309+182C>T
XR_001740206.1:n.870+182C>T
NM_002740.6:c.705+182C>T MANE Select NP_002731.4:n.705+182C>T
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