Canonical Allele Identifier: CA2695236262

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560854dup , CM000685.2:g.139560854dup	GRCh38
NC_000023.10:g.138643013dup , CM000685.1:g.138643013dup	GRCh37
NC_000023.9:g.138470679dup	NCBI36
NG_007994.1:g.35119dup , LRG_556:g.35119dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.837dup MANE Select	ENSP00000218099.2:p.Gly280ArgfsTer2
ENST00000643157.1:n.1504dup
ENST00000218099.6:c.837dup	ENSP00000218099.2:p.Gly280ArgfsTer2
ENST00000394090.2:c.723dup	ENSP00000377650.2:p.Gly242ArgfsTer2
NM_000133.3:c.837dup , LRG_556t1:c.837dup	NP_000124.1:p.Gly280ArgfsTer2
NM_001313913.1:c.723dup	NP_001300842.1:p.Gly242ArgfsTer2
XM_005262397.3:c.708dup	XP_005262454.1:p.Gly237ArgfsTer2
XM_005262397.4:c.708dup	XP_005262454.1:p.Gly237ArgfsTer2
NM_000133.4:c.837dup MANE Select	NP_000124.1:p.Gly280ArgfsTer2
NM_001313913.2:c.723dup	NP_001300842.1:p.Gly242ArgfsTer2