Canonical Allele Identifier: CA2695236269

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561535_139561537del , CM000685.2:g.139561535_139561537del	GRCh38
NC_000023.10:g.138643694_138643696del , CM000685.1:g.138643694_138643696del	GRCh37
NC_000023.9:g.138471360_138471362del	NCBI36
NG_007994.1:g.35800_35802del , LRG_556:g.35800_35802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.850_852del MANE Select	ENSP00000218099.2:p.Ile284del
ENST00000643157.1:n.1517_1519del
ENST00000218099.6:c.850_852del	ENSP00000218099.2:p.Ile284del
ENST00000394090.2:c.736_738del	ENSP00000377650.2:p.Ile246del
NM_000133.3:c.850_852del , LRG_556t1:c.850_852del	NP_000124.1:p.Ile284del
NM_001313913.1:c.736_738del	NP_001300842.1:p.Ile246del
XM_005262397.3:c.721_723del	XP_005262454.1:p.Ile241del
XM_005262397.4:c.721_723del	XP_005262454.1:p.Ile241del
NM_000133.4:c.850_852del MANE Select	NP_000124.1:p.Ile284del
NM_001313913.2:c.736_738del	NP_001300842.1:p.Ile246del