Canonical Allele Identifier: CA1929292132

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941788_94941798delinsTGCTAAATCAG , CM000672.2:g.94941788_94941798delinsTGCTAAATCAG	GRCh38
NC_000010.10:g.96701545_96701555delinsTGCTAAATCAG , CM000672.1:g.96701545_96701555delinsTGCTAAATCAG	GRCh37
NC_000010.9:g.96691535_96691545delinsTGCTAAATCAG	NCBI36
NG_008385.1:g.8131_8141delinsTGCTAAATCAG
NG_008385.2:g.8631_8641delinsTGCTAAATCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-70_169-60delinsTGCTAAATCAG MANE Select	ENSP00000260682.6:n.169-70_169-60delinsTGCTAAATCAG
ENST00000643112.1:c.169-70_169-60delinsTGCTAAATCAG	ENSP00000496202.1:n.169-70_169-60delinsTGCTAAATCAG
ENST00000645207.1:n.252_262delinsTGCTAAATCAG
ENST00000260682.6:c.169-70_169-60delinsTGCTAAATCAG	ENSP00000260682.6:n.169-70_169-60delinsTGCTAAATCAG
ENST00000461906.1:n.194-70_194-60delinsTGCTAAATCAG
NM_000771.3:c.169-70_169-60delinsTGCTAAATCAG	NP_000762.2:n.169-70_169-60delinsTGCTAAATCAG
NM_000771.4:c.169-70_169-60delinsTGCTAAATCAG MANE Select	NP_000762.2:n.169-70_169-60delinsTGCTAAATCAG