Canonical Allele Identifier: CA2461412289

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562003A= , CM000685.2:g.139562003A=	GRCh38
NC_000023.10:g.138644162A= , CM000685.1:g.138644162A=	GRCh37
NC_000023.9:g.138471828A=	NCBI36
NG_007994.1:g.36268A= , LRG_556:g.36268A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1318A= MANE Select	ENSP00000218099.2:p.Lys440=
ENST00000643157.1:n.1723+262A=
ENST00000218099.6:c.1318A=	ENSP00000218099.2:p.Lys440=
ENST00000394090.2:c.1204A=	ENSP00000377650.2:p.Lys402=
NM_000133.3:c.1318A= , LRG_556t1:c.1318A=	NP_000124.1:p.Lys440=
NM_001313913.1:c.1204A=	NP_001300842.1:p.Lys402=
XM_005262397.3:c.1189A=	XP_005262454.1:p.Lys397=
XM_005262397.4:c.1189A=	XP_005262454.1:p.Lys397=
NM_000133.4:c.1318A= MANE Select	NP_000124.1:p.Lys440=
NM_001313913.2:c.1204A=	NP_001300842.1:p.Lys402=