Canonical Allele Identifier: CA1929296076

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947337_94947339delinsCTT , CM000672.2:g.94947337_94947339delinsCTT	GRCh38
NC_000010.10:g.96707094_96707096delinsCTT , CM000672.1:g.96707094_96707096delinsCTT	GRCh37
NC_000010.9:g.96697084_96697086delinsCTT	NCBI36
NG_008385.1:g.13680_13682delinsCTT
NG_008385.2:g.14180_14182delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-442_482-440delinsCTT MANE Select	ENSP00000260682.6:n.482-442_482-440delinsCTT
ENST00000643112.1:c.482-442_482-440delinsCTT	ENSP00000496202.1:n.482-442_482-440delinsCTT
ENST00000645207.1:n.635-442_635-440delinsCTT
ENST00000260682.6:c.482-442_482-440delinsCTT	ENSP00000260682.6:n.482-442_482-440delinsCTT
ENST00000473496.1:n.253-442_253-440delinsCTT
NM_000771.3:c.482-442_482-440delinsCTT	NP_000762.2:n.482-442_482-440delinsCTT
NM_000771.4:c.482-442_482-440delinsCTT MANE Select	NP_000762.2:n.482-442_482-440delinsCTT