Canonical Allele Identifier: CA2695236401

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561943_139561944del , CM000685.2:g.139561943_139561944del	GRCh38
NC_000023.10:g.138644102_138644103del , CM000685.1:g.138644102_138644103del	GRCh37
NC_000023.9:g.138471768_138471769del	NCBI36
NG_007994.1:g.36208_36209del , LRG_556:g.36208_36209del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1258_1259del MANE Select	ENSP00000218099.2:p.Glu420ArgfsTer10
ENST00000643157.1:n.1723+202_1723+203del
ENST00000218099.6:c.1258_1259del	ENSP00000218099.2:p.Glu420ArgfsTer10
ENST00000394090.2:c.1144_1145del	ENSP00000377650.2:p.Glu382ArgfsTer10
NM_000133.3:c.1258_1259del , LRG_556t1:c.1258_1259del	NP_000124.1:p.Glu420ArgfsTer10
NM_001313913.1:c.1144_1145del	NP_001300842.1:p.Glu382ArgfsTer10
XM_005262397.3:c.1129_1130del	XP_005262454.1:p.Glu377ArgfsTer10
XM_005262397.4:c.1129_1130del	XP_005262454.1:p.Glu377ArgfsTer10
NM_000133.4:c.1258_1259del MANE Select	NP_000124.1:p.Glu420ArgfsTer10
NM_001313913.2:c.1144_1145del	NP_001300842.1:p.Glu382ArgfsTer10