Canonical Allele Identifier: CA2823819903

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548307_139548308insAAATAAA , CM000685.2:g.139548307_139548308insAAATAAA	GRCh38
NC_000023.10:g.138630466_138630467insAAATAAA , CM000685.1:g.138630466_138630467insAAATAAA	GRCh37
NC_000023.9:g.138458132_138458133insAAATAAA	NCBI36
NG_007994.1:g.22572_22573insAAATAAA , LRG_556:g.22572_22573insAAATAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-56_392-55insAAATAAA MANE Select	ENSP00000218099.2:n.392-56_392-55insAAATAAA
ENST00000643157.1:n.1059-56_1059-55insAAATAAA
ENST00000218099.6:c.392-56_392-55insAAATAAA	ENSP00000218099.2:n.392-56_392-55insAAATAAA
ENST00000394090.2:c.278-56_278-55insAAATAAA	ENSP00000377650.2:n.278-56_278-55insAAATAAA
ENST00000479617.2:n.345-56_345-55insAAATAAA
NM_000133.3:c.392-56_392-55insAAATAAA , LRG_556t1:c.392-56_392-55insAAATAAA	NP_000124.1:n.392-56_392-55insAAATAAA
NM_001313913.1:c.278-56_278-55insAAATAAA	NP_001300842.1:n.278-56_278-55insAAATAAA
XM_005262397.3:c.392-2755_392-2754insAAATAAA	XP_005262454.1:n.392-2755_392-2754insAAATAAA
XM_005262397.4:c.392-2755_392-2754insAAATAAA	XP_005262454.1:n.392-2755_392-2754insAAATAAA
NM_000133.4:c.392-56_392-55insAAATAAA MANE Select	NP_000124.1:n.392-56_392-55insAAATAAA
NM_001313913.2:c.278-56_278-55insAAATAAA	NP_001300842.1:n.278-56_278-55insAAATAAA