Canonical Allele Identifier: CA2521405902

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942089_94942090insCAAACGA , CM000672.2:g.94942089_94942090insCAAACGA	GRCh38
NC_000010.10:g.96701846_96701847insCAAACGA , CM000672.1:g.96701846_96701847insCAAACGA	GRCh37
NC_000010.9:g.96691836_96691837insCAAACGA	NCBI36
NG_008385.1:g.8432_8433insCAAACGA
NG_008385.2:g.8932_8933insCAAACGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.331+69_331+70insCAAACGA MANE Select	ENSP00000260682.6:n.331+69_331+70insCAAACGA
ENST00000643112.1:c.331+69_331+70insCAAACGA	ENSP00000496202.1:n.331+69_331+70insCAAACGA
ENST00000645207.1:n.484+69_484+70insCAAACGA
ENST00000260682.6:c.331+69_331+70insCAAACGA	ENSP00000260682.6:n.331+69_331+70insCAAACGA
ENST00000461906.1:n.356+69_356+70insCAAACGA
ENST00000473496.1:n.102+69_102+70insCAAACGA
NM_000771.3:c.331+69_331+70insCAAACGA	NP_000762.2:n.331+69_331+70insCAAACGA
NM_000771.4:c.331+69_331+70insCAAACGA MANE Select	NP_000762.2:n.331+69_331+70insCAAACGA