Canonical Allele Identifier: CA2695236387

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561908_139561910del , CM000685.2:g.139561908_139561910del	GRCh38
NC_000023.10:g.138644067_138644069del , CM000685.1:g.138644067_138644069del	GRCh37
NC_000023.9:g.138471733_138471735del	NCBI36
NG_007994.1:g.36173_36175del , LRG_556:g.36173_36175del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1223_1225del MANE Select	ENSP00000218099.2:p.Gln408_Gly409delinsArg
ENST00000643157.1:n.1723+167_1723+169del
ENST00000218099.6:c.1223_1225del	ENSP00000218099.2:p.Gln408_Gly409delinsArg
ENST00000394090.2:c.1109_1111del	ENSP00000377650.2:p.Gln370_Gly371delinsArg
NM_000133.3:c.1223_1225del , LRG_556t1:c.1223_1225del	NP_000124.1:p.Gln408_Gly409delinsArg
NM_001313913.1:c.1109_1111del	NP_001300842.1:p.Gln370_Gly371delinsArg
XM_005262397.3:c.1094_1096del	XP_005262454.1:p.Gln365_Gly366delinsArg
XM_005262397.4:c.1094_1096del	XP_005262454.1:p.Gln365_Gly366delinsArg
NM_000133.4:c.1223_1225del MANE Select	NP_000124.1:p.Gln408_Gly409delinsArg
NM_001313913.2:c.1109_1111del	NP_001300842.1:p.Gln370_Gly371delinsArg