Canonical Allele Identifier: CA2461408592

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551078_139551080delinsAAG , CM000685.2:g.139551078_139551080delinsAAG	GRCh38
NC_000023.10:g.138633237_138633239delinsAAG , CM000685.1:g.138633237_138633239delinsAAG	GRCh37
NC_000023.9:g.138460903_138460905delinsAAG	NCBI36
NG_007994.1:g.25343_25345delinsAAG , LRG_556:g.25343_25345delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.537_539delinsAAG MANE Select	ENSP00000218099.2:p.Gly179=
ENST00000643157.1:n.1204_1206delinsAAG
ENST00000218099.6:c.537_539delinsAAG	ENSP00000218099.2:p.Gly179=
ENST00000394090.2:c.423_425delinsAAG	ENSP00000377650.2:p.Gly141=
NM_000133.3:c.537_539delinsAAG , LRG_556t1:c.537_539delinsAAG	NP_000124.1:p.Gly179=
NM_001313913.1:c.423_425delinsAAG	NP_001300842.1:p.Gly141=
XM_005262397.3:c.408_410delinsAAG	XP_005262454.1:p.Gly136=
XM_005262397.4:c.408_410delinsAAG	XP_005262454.1:p.Gly136=
NM_000133.4:c.537_539delinsAAG MANE Select	NP_000124.1:p.Gly179=
NM_001313913.2:c.423_425delinsAAG	NP_001300842.1:p.Gly141=