Canonical Allele Identifier: CA1929335177

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974657_94974658delinsCA , CM000672.2:g.94974657_94974658delinsCA	GRCh38
NC_000010.10:g.96734414_96734415delinsCA , CM000672.1:g.96734414_96734415delinsCA	GRCh37
NC_000010.9:g.96724404_96724405delinsCA	NCBI36
NG_008385.1:g.41000_41001delinsCA
NG_008385.2:g.41500_41501delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2412_961+2413delinsCA MANE Select	ENSP00000260682.6:n.961+2412_961+2413delinsCA
ENST00000643112.1:c.820-6526_820-6525delinsCA	ENSP00000496202.1:n.820-6526_820-6525delinsCA
ENST00000260682.6:c.961+2412_961+2413delinsCA	ENSP00000260682.6:n.961+2412_961+2413delinsCA
NM_000771.3:c.961+2412_961+2413delinsCA	NP_000762.2:n.961+2412_961+2413delinsCA
NM_000771.4:c.961+2412_961+2413delinsCA MANE Select	NP_000762.2:n.961+2412_961+2413delinsCA