Canonical Allele Identifier: CA2789073519

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974525_94974526insTTTT , CM000672.2:g.94974525_94974526insTTTT	GRCh38
NC_000010.10:g.96734282_96734283insTTTT , CM000672.1:g.96734282_96734283insTTTT	GRCh37
NC_000010.9:g.96724272_96724273insTTTT	NCBI36
NG_008385.1:g.40868_40869insTTTT
NG_008385.2:g.41368_41369insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2280_961+2281insTTTT MANE Select	ENSP00000260682.6:n.961+2280_961+2281insTTTT
ENST00000643112.1:c.820-6658_820-6657insTTTT	ENSP00000496202.1:n.820-6658_820-6657insTTTT
ENST00000260682.6:c.961+2280_961+2281insTTTT	ENSP00000260682.6:n.961+2280_961+2281insTTTT
NM_000771.3:c.961+2280_961+2281insTTTT	NP_000762.2:n.961+2280_961+2281insTTTT
NM_000771.4:c.961+2280_961+2281insTTTT MANE Select	NP_000762.2:n.961+2280_961+2281insTTTT