Canonical Allele Identifier: CA1929341827

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981150_94981151delinsCT , CM000672.2:g.94981150_94981151delinsCT	GRCh38
NC_000010.10:g.96740907_96740908delinsCT , CM000672.1:g.96740907_96740908delinsCT	GRCh37
NC_000010.9:g.96730897_96730898delinsCT	NCBI36
NG_008385.1:g.47493_47494delinsCT
NG_008385.2:g.47993_47994delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.962-33_962-32delinsCT MANE Select	ENSP00000260682.6:n.962-33_962-32delinsCT
ENST00000643112.1:c.820-33_820-32delinsCT	ENSP00000496202.1:n.820-33_820-32delinsCT
ENST00000260682.6:c.962-33_962-32delinsCT	ENSP00000260682.6:n.962-33_962-32delinsCT
NM_000771.3:c.962-33_962-32delinsCT	NP_000762.2:n.962-33_962-32delinsCT
NM_000771.4:c.962-33_962-32delinsCT MANE Select	NP_000762.2:n.962-33_962-32delinsCT