Canonical Allele Identifier: CA2841394527
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139537147_139537148del , CM000685.2:g.139537147_139537148del GRCh38
NC_000023.10:g.138619306_138619307del , CM000685.1:g.138619306_138619307del GRCh37
NC_000023.9:g.138446972_138446973del NCBI36
NG_007994.1:g.11412_11413del , LRG_556:g.11412_11413del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.226_227del MANE Select ENSP00000218099.2:p.Glu76SerfsTer3
ENST00000218099.6:c.226_227del ENSP00000218099.2:p.Glu76SerfsTer3
ENST00000394090.2:c.226_227del ENSP00000377650.2:p.Glu76SerfsTer3
ENST00000479617.2:n.233_234del
NM_000133.3:c.226_227del , LRG_556t1:c.226_227del NP_000124.1:p.Glu76SerfsTer3
NM_001313913.1:c.226_227del NP_001300842.1:p.Glu76SerfsTer3
XM_005262397.3:c.226_227del XP_005262454.1:p.Glu76SerfsTer3
XM_005262397.4:c.226_227del XP_005262454.1:p.Glu76SerfsTer3
NM_000133.4:c.226_227del MANE Select NP_000124.1:p.Glu76SerfsTer3
NM_001313913.2:c.226_227del NP_001300842.1:p.Glu76SerfsTer3