Canonical Allele Identifier: CA2695236303

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561652_139561655del , CM000685.2:g.139561652_139561655del	GRCh38
NC_000023.10:g.138643811_138643814del , CM000685.1:g.138643811_138643814del	GRCh37
NC_000023.9:g.138471477_138471480del	NCBI36
NG_007994.1:g.35917_35920del , LRG_556:g.35917_35920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.967_970del MANE Select	ENSP00000218099.2:p.Glu323ProfsTer2
ENST00000643157.1:n.1634_1637del
ENST00000218099.6:c.967_970del	ENSP00000218099.2:p.Glu323ProfsTer2
ENST00000394090.2:c.853_856del	ENSP00000377650.2:p.Glu285ProfsTer2
NM_000133.3:c.967_970del , LRG_556t1:c.967_970del	NP_000124.1:p.Glu323ProfsTer2
NM_001313913.1:c.853_856del	NP_001300842.1:p.Glu285ProfsTer2
XM_005262397.3:c.838_841del	XP_005262454.1:p.Glu280ProfsTer2
XM_005262397.4:c.838_841del	XP_005262454.1:p.Glu280ProfsTer2
NM_000133.4:c.967_970del MANE Select	NP_000124.1:p.Glu323ProfsTer2
NM_001313913.2:c.853_856del	NP_001300842.1:p.Glu285ProfsTer2