Canonical Allele Identifier: CA2695236264

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561514_139561519del , CM000685.2:g.139561514_139561519del	GRCh38
NC_000023.10:g.138643673_138643678del , CM000685.1:g.138643673_138643678del	GRCh37
NC_000023.9:g.138471339_138471344del	NCBI36
NG_007994.1:g.35779_35784del , LRG_556:g.35779_35784del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.839-10_839-5del MANE Select	ENSP00000218099.2:n.839-10_839-5del
ENST00000643157.1:n.1506-10_1506-5del
ENST00000218099.6:c.839-10_839-5del	ENSP00000218099.2:n.839-10_839-5del
ENST00000394090.2:c.725-10_725-5del	ENSP00000377650.2:n.725-10_725-5del
NM_000133.3:c.839-10_839-5del , LRG_556t1:c.839-10_839-5del	NP_000124.1:n.839-10_839-5del
NM_001313913.1:c.725-10_725-5del	NP_001300842.1:n.725-10_725-5del
XM_005262397.3:c.710-10_710-5del	XP_005262454.1:n.710-10_710-5del
XM_005262397.4:c.710-10_710-5del	XP_005262454.1:n.710-10_710-5del
NM_000133.4:c.839-10_839-5del MANE Select	NP_000124.1:n.839-10_839-5del
NM_001313913.2:c.725-10_725-5del	NP_001300842.1:n.725-10_725-5del