Canonical Allele Identifier: CA2610267797
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942320del , CM000672.2:g.94942320del GRCh38
NC_000010.10:g.96702077del , CM000672.1:g.96702077del GRCh37
NC_000010.9:g.96692067del NCBI36
NG_008385.1:g.8663del
NG_008385.2:g.9163del

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.460del MANE Select ENSP00000260682.6:p.Glu154ArgfsTer3
ENST00000643112.1:c.460del ENSP00000496202.1:p.Glu154ArgfsTer3
ENST00000645207.1:n.613del
ENST00000260682.6:c.460del ENSP00000260682.6:p.Glu154ArgfsTer3
ENST00000461906.1:n.485del
ENST00000473496.1:n.231del
NM_000771.3:c.460del NP_000762.2:p.Glu154ArgfsTer3
NM_000771.4:c.460del MANE Select NP_000762.2:p.Glu154ArgfsTer3