Canonical Allele Identifier: CA1929296246

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947513_94947522delinsCCTTTTTGTT , CM000672.2:g.94947513_94947522delinsCCTTTTTGTT	GRCh38
NC_000010.10:g.96707270_96707279delinsCCTTTTTGTT , CM000672.1:g.96707270_96707279delinsCCTTTTTGTT	GRCh37
NC_000010.9:g.96697260_96697269delinsCCTTTTTGTT	NCBI36
NG_008385.1:g.13856_13865delinsCCTTTTTGTT
NG_008385.2:g.14356_14365delinsCCTTTTTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-266_482-257delinsCCTTTTTGTT MANE Select	ENSP00000260682.6:n.482-266_482-257delinsCCTTTTTGTT
ENST00000643112.1:c.482-266_482-257delinsCCTTTTTGTT	ENSP00000496202.1:n.482-266_482-257delinsCCTTTTTGTT
ENST00000645207.1:n.635-266_635-257delinsCCTTTTTGTT
ENST00000260682.6:c.482-266_482-257delinsCCTTTTTGTT	ENSP00000260682.6:n.482-266_482-257delinsCCTTTTTGTT
ENST00000473496.1:n.253-266_253-257delinsCCTTTTTGTT
NM_000771.3:c.482-266_482-257delinsCCTTTTTGTT	NP_000762.2:n.482-266_482-257delinsCCTTTTTGTT
NM_000771.4:c.482-266_482-257delinsCCTTTTTGTT MANE Select	NP_000762.2:n.482-266_482-257delinsCCTTTTTGTT