Canonical Allele Identifier: CA2695236270

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561541_139561543del , CM000685.2:g.139561541_139561543del	GRCh38
NC_000023.10:g.138643700_138643702del , CM000685.1:g.138643700_138643702del	GRCh37
NC_000023.9:g.138471366_138471368del	NCBI36
NG_007994.1:g.35806_35808del , LRG_556:g.35806_35808del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.856_858del MANE Select	ENSP00000218099.2:p.Glu286del
ENST00000643157.1:n.1523_1525del
ENST00000218099.6:c.856_858del	ENSP00000218099.2:p.Glu286del
ENST00000394090.2:c.742_744del	ENSP00000377650.2:p.Glu248del
NM_000133.3:c.856_858del , LRG_556t1:c.856_858del	NP_000124.1:p.Glu286del
NM_001313913.1:c.742_744del	NP_001300842.1:p.Glu248del
XM_005262397.3:c.727_729del	XP_005262454.1:p.Glu243del
XM_005262397.4:c.727_729del	XP_005262454.1:p.Glu243del
NM_000133.4:c.856_858del MANE Select	NP_000124.1:p.Glu286del
NM_001313913.2:c.742_744del	NP_001300842.1:p.Glu248del