Canonical Allele Identifier: CA2695236313

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541152_139541154dup , CM000685.2:g.139541152_139541154dup	GRCh38
NC_000023.10:g.138623311_138623313dup , CM000685.1:g.138623311_138623313dup	GRCh37
NC_000023.9:g.138450977_138450979dup	NCBI36
NG_007994.1:g.15417_15419dup , LRG_556:g.15417_15419dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.354_356dup MANE Select	ENSP00000218099.2:p.Trp118_Cys119insTrp
ENST00000218099.6:c.354_356dup	ENSP00000218099.2:p.Trp118_Cys119insTrp
ENST00000394090.2:c.277+3766_277+3768dup	ENSP00000377650.2:n.277+3766_277+3768dup
ENST00000479617.2:n.307_309dup
NM_000133.3:c.354_356dup , LRG_556t1:c.354_356dup	NP_000124.1:p.Trp118_Cys119insTrp
NM_001313913.1:c.277+3766_277+3768dup	NP_001300842.1:n.277+3766_277+3768dup
XM_005262397.3:c.354_356dup	XP_005262454.1:p.Trp118_Cys119insTrp
XM_005262397.4:c.354_356dup	XP_005262454.1:p.Trp118_Cys119insTrp
NM_000133.4:c.354_356dup MANE Select	NP_000124.1:p.Trp118_Cys119insTrp
NM_001313913.2:c.277+3766_277+3768dup	NP_001300842.1:n.277+3766_277+3768dup