Canonical Allele Identifier: CA2830550881
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988961_94988962del , CM000672.2:g.94988961_94988962del GRCh38
NC_000010.10:g.96748718_96748719del , CM000672.1:g.96748718_96748719del GRCh37
NC_000010.9:g.96738708_96738709del NCBI36
NG_008385.1:g.55304_55305del
NG_008385.2:g.55804_55805del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1406_1407del MANE Select ENSP00000260682.6:p.Thr469AsnfsTer?
ENST00000643112.1:c.*415_*416del ENSP00000496202.1:n.*415_*416del
ENST00000260682.6:c.1406_1407del ENSP00000260682.6:p.Thr469AsnfsTer?
NM_000771.3:c.1406_1407del NP_000762.2:p.Thr469AsnfsTer?
NM_000771.4:c.1406_1407del MANE Select NP_000762.2:p.Thr469AsnfsTer?