Canonical Allele Identifier: CA1929292447
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942305_94942306delinsGC , CM000672.2:g.94942305_94942306delinsGC GRCh38
NC_000010.10:g.96702062_96702063delinsGC , CM000672.1:g.96702062_96702063delinsGC GRCh37
NC_000010.9:g.96692052_96692053delinsGC NCBI36
NG_008385.1:g.8648_8649delinsGC
NG_008385.2:g.9148_9149delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.445_446delinsGC MANE Select ENSP00000260682.6:p.Ala149=
ENST00000643112.1:c.445_446delinsGC ENSP00000496202.1:p.Ala149=
ENST00000645207.1:n.598_599delinsGC
ENST00000260682.6:c.445_446delinsGC ENSP00000260682.6:p.Ala149=
ENST00000461906.1:n.470_471delinsGC
ENST00000473496.1:n.216_217delinsGC
NM_000771.3:c.445_446delinsGC NP_000762.2:p.Ala149=
NM_000771.4:c.445_446delinsGC MANE Select NP_000762.2:p.Ala149=
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