Canonical Allele Identifier: CA1929292366
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942161_94942162delinsTC , CM000672.2:g.94942161_94942162delinsTC GRCh38
NC_000010.10:g.96701918_96701919delinsTC , CM000672.1:g.96701918_96701919delinsTC GRCh37
NC_000010.9:g.96691908_96691909delinsTC NCBI36
NG_008385.1:g.8504_8505delinsTC
NG_008385.2:g.9004_9005delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.332-31_332-30delinsTC MANE Select ENSP00000260682.6:n.332-31_332-30delinsTC
ENST00000643112.1:c.332-31_332-30delinsTC ENSP00000496202.1:n.332-31_332-30delinsTC
ENST00000645207.1:n.485-31_485-30delinsTC
ENST00000260682.6:c.332-31_332-30delinsTC ENSP00000260682.6:n.332-31_332-30delinsTC
ENST00000461906.1:n.357-31_357-30delinsTC
ENST00000473496.1:n.103-31_103-30delinsTC
NM_000771.3:c.332-31_332-30delinsTC NP_000762.2:n.332-31_332-30delinsTC
NM_000771.4:c.332-31_332-30delinsTC MANE Select NP_000762.2:n.332-31_332-30delinsTC