Canonical Allele Identifier: CA1929296291

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947566_94947567delinsCA , CM000672.2:g.94947566_94947567delinsCA	GRCh38
NC_000010.10:g.96707323_96707324delinsCA , CM000672.1:g.96707323_96707324delinsCA	GRCh37
NC_000010.9:g.96697313_96697314delinsCA	NCBI36
NG_008385.1:g.13909_13910delinsCA
NG_008385.2:g.14409_14410delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-213_482-212delinsCA MANE Select	ENSP00000260682.6:n.482-213_482-212delinsCA
ENST00000643112.1:c.482-213_482-212delinsCA	ENSP00000496202.1:n.482-213_482-212delinsCA
ENST00000645207.1:n.635-213_635-212delinsCA
ENST00000260682.6:c.482-213_482-212delinsCA	ENSP00000260682.6:n.482-213_482-212delinsCA
ENST00000473496.1:n.253-213_253-212delinsCA
NM_000771.3:c.482-213_482-212delinsCA	NP_000762.2:n.482-213_482-212delinsCA
NM_000771.4:c.482-213_482-212delinsCA MANE Select	NP_000762.2:n.482-213_482-212delinsCA