Canonical Allele Identifier: CA2695236416

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562013_139562021dup , CM000685.2:g.139562013_139562021dup	GRCh38
NC_000023.10:g.138644172_138644180dup , CM000685.1:g.138644172_138644180dup	GRCh37
NC_000023.9:g.138471838_138471846dup	NCBI36
NG_007994.1:g.36278_36286dup , LRG_556:g.36278_36286dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1328_1336dup MANE Select	ENSP00000218099.2:p.Thr445_Lys446insIleTy...
ENST00000643157.1:n.1723+272_1723+280dup
ENST00000218099.6:c.1328_1336dup	ENSP00000218099.2:p.Thr445_Lys446insIleTy...
ENST00000394090.2:c.1214_1222dup	ENSP00000377650.2:p.Thr407_Lys408insIleTy...
NM_000133.3:c.1328_1336dup , LRG_556t1:c.1328_1336dup	NP_000124.1:p.Thr445_Lys446insIleTyrThr
NM_001313913.1:c.1214_1222dup	NP_001300842.1:p.Thr407_Lys408insIleTyrTh...
XM_005262397.3:c.1199_1207dup	XP_005262454.1:p.Thr402_Lys403insIleTyrTh...
XM_005262397.4:c.1199_1207dup	XP_005262454.1:p.Thr402_Lys403insIleTyrTh...
NM_000133.4:c.1328_1336dup MANE Select	NP_000124.1:p.Thr445_Lys446insIleTyrThr
NM_001313913.2:c.1214_1222dup	NP_001300842.1:p.Thr407_Lys408insIleTyrTh...