Canonical Allele Identifier: CA2695236361

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561844_139561845dup , CM000685.2:g.139561844_139561845dup	GRCh38
NC_000023.10:g.138644003_138644004dup , CM000685.1:g.138644003_138644004dup	GRCh37
NC_000023.9:g.138471669_138471670dup	NCBI36
NG_007994.1:g.36109_36110dup , LRG_556:g.36109_36110dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1159_1160dup MANE Select	ENSP00000218099.2:p.Phe388SerfsTer?
ENST00000643157.1:n.1723+103_1723+104dup
ENST00000218099.6:c.1159_1160dup	ENSP00000218099.2:p.Phe388SerfsTer?
ENST00000394090.2:c.1045_1046dup	ENSP00000377650.2:p.Phe350SerfsTer?
NM_000133.3:c.1159_1160dup , LRG_556t1:c.1159_1160dup	NP_000124.1:p.Phe388SerfsTer?
NM_001313913.1:c.1045_1046dup	NP_001300842.1:p.Phe350SerfsTer?
XM_005262397.3:c.1030_1031dup	XP_005262454.1:p.Phe345SerfsTer?
XM_005262397.4:c.1030_1031dup	XP_005262454.1:p.Phe345SerfsTer?
NM_000133.4:c.1159_1160dup MANE Select	NP_000124.1:p.Phe388SerfsTer?
NM_001313913.2:c.1045_1046dup	NP_001300842.1:p.Phe350SerfsTer?