Canonical Allele Identifier: CA2461408603

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551115_139551130delinsGCTGAGACTGTTTTTC , CM000685.2:g.139551115_139551130delinsGCTGAGACTGTTTTTC	GRCh38
NC_000023.10:g.138633274_138633289delinsGCTGAGACTGTTTTTC , CM000685.1:g.138633274_138633289delinsGCTGAGACTGTTTTTC	GRCh37
NC_000023.9:g.138460940_138460955delinsGCTGAGACTGTTTTTC	NCBI36
NG_007994.1:g.25380_25395delinsGCTGAGACTGTTTTTC , LRG_556:g.25380_25395delinsGCTGAGACTGTTTTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.574_589delinsGCTGAGACTGTTTTTC MANE Select	ENSP00000218099.2:p.Ala192=
ENST00000643157.1:n.1241_1256delinsGCTGAGACTGTTTTTC
ENST00000218099.6:c.574_589delinsGCTGAGACTGTTTTTC	ENSP00000218099.2:p.Ala192=
ENST00000394090.2:c.460_475delinsGCTGAGACTGTTTTTC	ENSP00000377650.2:p.Ala154=
NM_000133.3:c.574_589delinsGCTGAGACTGTTTTTC , LRG_556t1:c.574_589delinsGCTGAGACTGTTTTTC	NP_000124.1:p.Ala192=
NM_001313913.1:c.460_475delinsGCTGAGACTGTTTTTC	NP_001300842.1:p.Ala154=
XM_005262397.3:c.445_460delinsGCTGAGACTGTTTTTC	XP_005262454.1:p.Ala149=
XM_005262397.4:c.445_460delinsGCTGAGACTGTTTTTC	XP_005262454.1:p.Ala149=
NM_000133.4:c.574_589delinsGCTGAGACTGTTTTTC MANE Select	NP_000124.1:p.Ala192=
NM_001313913.2:c.460_475delinsGCTGAGACTGTTTTTC	NP_001300842.1:p.Ala154=