Canonical Allele Identifier: CA653577639

Gene: CYP2C9

Linked Data

• COSMIC: COSN17075716

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94989184_94989185insA , CM000672.2:g.94989184_94989185insA	GRCh38
NC_000010.10:g.96748941_96748942insA , CM000672.1:g.96748941_96748942insA	GRCh37
NC_000010.9:g.96738931_96738932insA	NCBI36
NG_008385.1:g.55527_55528insA
NG_008385.2:g.56027_56028insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.*156_*157insA MANE Select	ENSP00000260682.6:n.*156_*157insA
ENST00000643112.1:c.*638_*639insA	ENSP00000496202.1:n.*638_*639insA
ENST00000260682.6:c.*156_*157insA	ENSP00000260682.6:n.*156_*157insA
NM_000771.3:c.*156_*157insA	NP_000762.2:n.*156_*157insA
NM_000771.4:c.*156_*157insA MANE Select	NP_000762.2:n.*156_*157insA