Canonical Allele Identifier: CA645557375
Gene: CYP2C9 HGNC NCBI

Linked Data

COSMIC: COSM265613
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949118_94949119insG , CM000672.2:g.94949118_94949119insG GRCh38
NC_000010.10:g.96708875_96708876insG , CM000672.1:g.96708875_96708876insG GRCh37
NC_000010.9:g.96698865_96698866insG NCBI36
NG_008385.1:g.15461_15462insG
NG_008385.2:g.15961_15962insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.653_654insG MANE Select ENSP00000260682.6:p.Asn218LysfsTer7
ENST00000643112.1:c.653_654insG ENSP00000496202.1:p.Asn218LysfsTer7
ENST00000260682.6:c.653_654insG ENSP00000260682.6:p.Asn218LysfsTer7
ENST00000473496.1:n.424_425insG
NM_000771.3:c.653_654insG NP_000762.2:p.Asn218LysfsTer7
NM_000771.4:c.653_654insG MANE Select NP_000762.2:p.Asn218LysfsTer7
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