Canonical Allele Identifier: CA2695236424
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562044_139562047dup , CM000685.2:g.139562044_139562047dup GRCh38
NC_000023.10:g.138644203_138644206dup , CM000685.1:g.138644203_138644206dup GRCh37
NC_000023.9:g.138471869_138471872dup NCBI36
NG_007994.1:g.36309_36312dup , LRG_556:g.36309_36312dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.1359_1362dup MANE Select ENSP00000218099.2:p.Lys455AspfsTer2
ENST00000643157.1:n.1723+303_1723+306dup
ENST00000218099.6:c.1359_1362dup ENSP00000218099.2:p.Lys455AspfsTer2
ENST00000394090.2:c.1245_1248dup ENSP00000377650.2:p.Lys417AspfsTer2
NM_000133.3:c.1359_1362dup , LRG_556t1:c.1359_1362dup NP_000124.1:p.Lys455AspfsTer2
NM_001313913.1:c.1245_1248dup NP_001300842.1:p.Lys417AspfsTer2
XM_005262397.3:c.1230_1233dup XP_005262454.1:p.Lys412AspfsTer2
XM_005262397.4:c.1230_1233dup XP_005262454.1:p.Lys412AspfsTer2
NM_000133.4:c.1359_1362dup MANE Select NP_000124.1:p.Lys455AspfsTer2
NM_001313913.2:c.1245_1248dup NP_001300842.1:p.Lys417AspfsTer2