Canonical Allele Identifier: CA2695236327

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561739dup , CM000685.2:g.139561739dup	GRCh38
NC_000023.10:g.138643898dup , CM000685.1:g.138643898dup	GRCh37
NC_000023.9:g.138471564dup	NCBI36
NG_007994.1:g.36004dup , LRG_556:g.36004dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1054dup MANE Select	ENSP00000218099.2:p.Tyr352LeufsTer22
ENST00000643157.1:n.1721dup
ENST00000218099.6:c.1054dup	ENSP00000218099.2:p.Tyr352LeufsTer22
ENST00000394090.2:c.940dup	ENSP00000377650.2:p.Tyr314LeufsTer22
NM_000133.3:c.1054dup , LRG_556t1:c.1054dup	NP_000124.1:p.Tyr352LeufsTer22
NM_001313913.1:c.940dup	NP_001300842.1:p.Tyr314LeufsTer22
XM_005262397.3:c.925dup	XP_005262454.1:p.Tyr309LeufsTer22
XM_005262397.4:c.925dup	XP_005262454.1:p.Tyr309LeufsTer22
NM_000133.4:c.1054dup MANE Select	NP_000124.1:p.Tyr352LeufsTer22
NM_001313913.2:c.940dup	NP_001300842.1:p.Tyr314LeufsTer22