Canonical Allele Identifier: CA2695236271

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561547_139561548del , CM000685.2:g.139561547_139561548del	GRCh38
NC_000023.10:g.138643706_138643707del , CM000685.1:g.138643706_138643707del	GRCh37
NC_000023.9:g.138471372_138471373del	NCBI36
NG_007994.1:g.35812_35813del , LRG_556:g.35812_35813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.862_863del MANE Select	ENSP00000218099.2:p.Glu288ThrfsTer22
ENST00000643157.1:n.1529_1530del
ENST00000218099.6:c.862_863del	ENSP00000218099.2:p.Glu288ThrfsTer22
ENST00000394090.2:c.748_749del	ENSP00000377650.2:p.Glu250ThrfsTer22
NM_000133.3:c.862_863del , LRG_556t1:c.862_863del	NP_000124.1:p.Glu288ThrfsTer22
NM_001313913.1:c.748_749del	NP_001300842.1:p.Glu250ThrfsTer22
XM_005262397.3:c.733_734del	XP_005262454.1:p.Glu245ThrfsTer22
XM_005262397.4:c.733_734del	XP_005262454.1:p.Glu245ThrfsTer22
NM_000133.4:c.862_863del MANE Select	NP_000124.1:p.Glu288ThrfsTer22
NM_001313913.2:c.748_749del	NP_001300842.1:p.Glu250ThrfsTer22