Canonical Allele Identifier: CA2461404275

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537079_139537081delinsAAG , CM000685.2:g.139537079_139537081delinsAAG	GRCh38
NC_000023.10:g.138619238_138619240delinsAAG , CM000685.1:g.138619238_138619240delinsAAG	GRCh37
NC_000023.9:g.138446904_138446906delinsAAG	NCBI36
NG_007994.1:g.11344_11346delinsAAG , LRG_556:g.11344_11346delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.158_160delinsAAG MANE Select	ENSP00000218099.2:p.Glu53=
ENST00000218099.6:c.158_160delinsAAG	ENSP00000218099.2:p.Glu53=
ENST00000394090.2:c.158_160delinsAAG	ENSP00000377650.2:p.Glu53=
ENST00000479617.2:n.165_167delinsAAG
NM_000133.3:c.158_160delinsAAG , LRG_556t1:c.158_160delinsAAG	NP_000124.1:p.Glu53=
NM_001313913.1:c.158_160delinsAAG	NP_001300842.1:p.Glu53=
XM_005262397.3:c.158_160delinsAAG	XP_005262454.1:p.Glu53=
XM_005262397.4:c.158_160delinsAAG	XP_005262454.1:p.Glu53=
NM_000133.4:c.158_160delinsAAG MANE Select	NP_000124.1:p.Glu53=
NM_001313913.2:c.158_160delinsAAG	NP_001300842.1:p.Glu53=