Canonical Allele Identifier: CA2695236417
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562016_139562027dup , CM000685.2:g.139562016_139562027dup GRCh38
NC_000023.10:g.138644175_138644186dup , CM000685.1:g.138644175_138644186dup GRCh37
NC_000023.9:g.138471841_138471852dup NCBI36
NG_007994.1:g.36281_36292dup , LRG_556:g.36281_36292dup

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1331_1342dup MANE Select ENSP00000218099.2:p.Val447_Ser448insTyrTh...
ENST00000643157.1:n.1723+275_1723+286dup
ENST00000218099.6:c.1331_1342dup ENSP00000218099.2:p.Val447_Ser448insTyrTh...
ENST00000394090.2:c.1217_1228dup ENSP00000377650.2:p.Val409_Ser410insTyrTh...
NM_000133.3:c.1331_1342dup , LRG_556t1:c.1331_1342dup NP_000124.1:p.Val447_Ser448insTyrThrLysVa...
NM_001313913.1:c.1217_1228dup NP_001300842.1:p.Val409_Ser410insTyrThrLy...
XM_005262397.3:c.1202_1213dup XP_005262454.1:p.Val404_Ser405insTyrThrLy...
XM_005262397.4:c.1202_1213dup XP_005262454.1:p.Val404_Ser405insTyrThrLy...
NM_000133.4:c.1331_1342dup MANE Select NP_000124.1:p.Val447_Ser448insTyrThrLysVa...
NM_001313913.2:c.1217_1228dup NP_001300842.1:p.Val409_Ser410insTyrThrLy...