Canonical Allele Identifier: CA2461411811

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560757A= , CM000685.2:g.139560757A=	GRCh38
NC_000023.10:g.138642916A= , CM000685.1:g.138642916A=	GRCh37
NC_000023.9:g.138470582A=	NCBI36
NG_007994.1:g.35022A= , LRG_556:g.35022A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.740A= MANE Select	ENSP00000218099.2:p.Lys247=
ENST00000643157.1:n.1407A=
ENST00000218099.6:c.740A=	ENSP00000218099.2:p.Lys247=
ENST00000394090.2:c.626A=	ENSP00000377650.2:p.Lys209=
NM_000133.3:c.740A= , LRG_556t1:c.740A=	NP_000124.1:p.Lys247=
NM_001313913.1:c.626A=	NP_001300842.1:p.Lys209=
XM_005262397.3:c.611A=	XP_005262454.1:p.Lys204=
XM_005262397.4:c.611A=	XP_005262454.1:p.Lys204=
NM_000133.4:c.740A= MANE Select	NP_000124.1:p.Lys247=
NM_001313913.2:c.626A=	NP_001300842.1:p.Lys209=