Canonical Allele Identifier: CA1929292597

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942578_94942579delinsTC , CM000672.2:g.94942578_94942579delinsTC	GRCh38
NC_000010.10:g.96702335_96702336delinsTC , CM000672.1:g.96702335_96702336delinsTC	GRCh37
NC_000010.9:g.96692325_96692326delinsTC	NCBI36
NG_008385.1:g.8921_8922delinsTC
NG_008385.2:g.9421_9422delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+237_481+238delinsTC MANE Select	ENSP00000260682.6:n.481+237_481+238delinsTC
ENST00000643112.1:c.481+237_481+238delinsTC	ENSP00000496202.1:n.481+237_481+238delinsTC
ENST00000645207.1:n.634+237_634+238delinsTC
ENST00000260682.6:c.481+237_481+238delinsTC	ENSP00000260682.6:n.481+237_481+238delinsTC
ENST00000461906.1:n.743_744delinsTC
ENST00000473496.1:n.252+237_252+238delinsTC
NM_000771.3:c.481+237_481+238delinsTC	NP_000762.2:n.481+237_481+238delinsTC
NM_000771.4:c.481+237_481+238delinsTC MANE Select	NP_000762.2:n.481+237_481+238delinsTC