Canonical Allele Identifier: CA1929292158

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941833_94941836delinsCTGT , CM000672.2:g.94941833_94941836delinsCTGT	GRCh38
NC_000010.10:g.96701590_96701593delinsCTGT , CM000672.1:g.96701590_96701593delinsCTGT	GRCh37
NC_000010.9:g.96691580_96691583delinsCTGT	NCBI36
NG_008385.1:g.8176_8179delinsCTGT
NG_008385.2:g.8676_8679delinsCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-25_169-22delinsCTGT MANE Select	ENSP00000260682.6:n.169-25_169-22delinsCTGT
ENST00000643112.1:c.169-25_169-22delinsCTGT	ENSP00000496202.1:n.169-25_169-22delinsCTGT
ENST00000645207.1:n.297_300delinsCTGT
ENST00000260682.6:c.169-25_169-22delinsCTGT	ENSP00000260682.6:n.169-25_169-22delinsCTGT
ENST00000461906.1:n.194-25_194-22delinsCTGT
NM_000771.3:c.169-25_169-22delinsCTGT	NP_000762.2:n.169-25_169-22delinsCTGT
NM_000771.4:c.169-25_169-22delinsCTGT MANE Select	NP_000762.2:n.169-25_169-22delinsCTGT