Canonical Allele Identifier: CA1929292494

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942387_94942389delinsTTC , CM000672.2:g.94942387_94942389delinsTTC	GRCh38
NC_000010.10:g.96702144_96702146delinsTTC , CM000672.1:g.96702144_96702146delinsTTC	GRCh37
NC_000010.9:g.96692134_96692136delinsTTC	NCBI36
NG_008385.1:g.8730_8732delinsTTC
NG_008385.2:g.9230_9232delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+46_481+48delinsTTC MANE Select	ENSP00000260682.6:n.481+46_481+48delinsTTC
ENST00000643112.1:c.481+46_481+48delinsTTC	ENSP00000496202.1:n.481+46_481+48delinsTTC
ENST00000645207.1:n.634+46_634+48delinsTTC
ENST00000260682.6:c.481+46_481+48delinsTTC	ENSP00000260682.6:n.481+46_481+48delinsTTC
ENST00000461906.1:n.552_554delinsTTC
ENST00000473496.1:n.252+46_252+48delinsTTC
NM_000771.3:c.481+46_481+48delinsTTC	NP_000762.2:n.481+46_481+48delinsTTC
NM_000771.4:c.481+46_481+48delinsTTC MANE Select	NP_000762.2:n.481+46_481+48delinsTTC