Canonical Allele Identifier: CA2695236152

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537039dup , CM000685.2:g.139537039dup	GRCh38
NC_000023.10:g.138619198dup , CM000685.1:g.138619198dup	GRCh37
NC_000023.9:g.138446864dup	NCBI36
NG_007994.1:g.11304dup , LRG_556:g.11304dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.118dup MANE Select	ENSP00000218099.2:p.Ile40AsnfsTer9
ENST00000218099.6:c.118dup	ENSP00000218099.2:p.Ile40AsnfsTer9
ENST00000394090.2:c.118dup	ENSP00000377650.2:p.Ile40AsnfsTer9
ENST00000479617.2:n.125dup
NM_000133.3:c.118dup , LRG_556t1:c.118dup	NP_000124.1:p.Ile40AsnfsTer9
NM_001313913.1:c.118dup	NP_001300842.1:p.Ile40AsnfsTer9
XM_005262397.3:c.118dup	XP_005262454.1:p.Ile40AsnfsTer9
XM_005262397.4:c.118dup	XP_005262454.1:p.Ile40AsnfsTer9
NM_000133.4:c.118dup MANE Select	NP_000124.1:p.Ile40AsnfsTer9
NM_001313913.2:c.118dup	NP_001300842.1:p.Ile40AsnfsTer9