Canonical Allele Identifier: CA1929349580
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988888_94988890delinsCTG , CM000672.2:g.94988888_94988890delinsCTG GRCh38
NC_000010.10:g.96748645_96748647delinsCTG , CM000672.1:g.96748645_96748647delinsCTG GRCh37
NC_000010.9:g.96738635_96738637delinsCTG NCBI36
NG_008385.1:g.55231_55233delinsCTG
NG_008385.2:g.55731_55733delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1333_1335delinsCTG MANE Select ENSP00000260682.6:p.Leu445=
ENST00000643112.1:c.*342_*344delinsCTG ENSP00000496202.1:n.*342_*344delinsCTG
ENST00000260682.6:c.1333_1335delinsCTG ENSP00000260682.6:p.Leu445=
NM_000771.3:c.1333_1335delinsCTG NP_000762.2:p.Leu445=
NM_000771.4:c.1333_1335delinsCTG MANE Select NP_000762.2:p.Leu445=
Search 100 bp 5'
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