Canonical Allele Identifier: CA1929292185
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941883_94941885delinsTCA , CM000672.2:g.94941883_94941885delinsTCA GRCh38
NC_000010.10:g.96701640_96701642delinsTCA , CM000672.1:g.96701640_96701642delinsTCA GRCh37
NC_000010.9:g.96691630_96691632delinsTCA NCBI36
NG_008385.1:g.8226_8228delinsTCA
NG_008385.2:g.8726_8728delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.194_196delinsTCA MANE Select ENSP00000260682.6:p.Phe65=
ENST00000643112.1:c.194_196delinsTCA ENSP00000496202.1:p.Phe65=
ENST00000645207.1:n.347_349delinsTCA
ENST00000260682.6:c.194_196delinsTCA ENSP00000260682.6:p.Phe65=
ENST00000461906.1:n.219_221delinsTCA
NM_000771.3:c.194_196delinsTCA NP_000762.2:p.Phe65=
NM_000771.4:c.194_196delinsTCA MANE Select NP_000762.2:p.Phe65=
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