Canonical Allele Identifier: CA2461407788

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548404T= , CM000685.2:g.139548404T=	GRCh38
NC_000023.10:g.138630563T= , CM000685.1:g.138630563T=	GRCh37
NC_000023.9:g.138458229T=	NCBI36
NG_007994.1:g.22669T= , LRG_556:g.22669T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.433T= MANE Select	ENSP00000218099.2:p.Cys145=
ENST00000643157.1:n.1100T=
ENST00000218099.6:c.433T=	ENSP00000218099.2:p.Cys145=
ENST00000394090.2:c.319T=	ENSP00000377650.2:p.Cys107=
NM_000133.3:c.433T= , LRG_556t1:c.433T=	NP_000124.1:p.Cys145=
NM_001313913.1:c.319T=	NP_001300842.1:p.Cys107=
XM_005262397.3:c.392-2658T=	XP_005262454.1:n.392-2658T=
XM_005262397.4:c.392-2658T=	XP_005262454.1:n.392-2658T=
NM_000133.4:c.433T= MANE Select	NP_000124.1:p.Cys145=
NM_001313913.2:c.319T=	NP_001300842.1:p.Cys107=