Canonical Allele Identifier: CA1929295949

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947193_94947195delinsCTA , CM000672.2:g.94947193_94947195delinsCTA	GRCh38
NC_000010.10:g.96706950_96706952delinsCTA , CM000672.1:g.96706950_96706952delinsCTA	GRCh37
NC_000010.9:g.96696940_96696942delinsCTA	NCBI36
NG_008385.1:g.13536_13538delinsCTA
NG_008385.2:g.14036_14038delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-586_482-584delinsCTA MANE Select	ENSP00000260682.6:n.482-586_482-584delinsCTA
ENST00000643112.1:c.482-586_482-584delinsCTA	ENSP00000496202.1:n.482-586_482-584delinsCTA
ENST00000645207.1:n.635-586_635-584delinsCTA
ENST00000260682.6:c.482-586_482-584delinsCTA	ENSP00000260682.6:n.482-586_482-584delinsCTA
ENST00000473496.1:n.253-586_253-584delinsCTA
NM_000771.3:c.482-586_482-584delinsCTA	NP_000762.2:n.482-586_482-584delinsCTA
NM_000771.4:c.482-586_482-584delinsCTA MANE Select	NP_000762.2:n.482-586_482-584delinsCTA