Canonical Allele Identifier: CA2461412241

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561916A= , CM000685.2:g.139561916A=	GRCh38
NC_000023.10:g.138644075A= , CM000685.1:g.138644075A=	GRCh37
NC_000023.9:g.138471741A=	NCBI36
NG_007994.1:g.36181A= , LRG_556:g.36181A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.1231A= MANE Select	NP_000124.1:p.Ser411=
ENST00000218099.7:c.1231A= MANE Select	ENSP00000218099.2:p.Ser411=
NM_000133.3:c.1231A= , LRG_556t1:c.1231A=	NP_000124.1:p.Ser411=
NM_001313913.1:c.1117A=	NP_001300842.1:p.Ser373=
NM_001313913.2:c.1117A=	NP_001300842.1:p.Ser373=
ENST00000218099.6:c.1231A=	ENSP00000218099.2:p.Ser411=
ENST00000394090.2:c.1117A=	ENSP00000377650.2:p.Ser373=
ENST00000643157.1:n.1723+175A=
XM_005262397.3:c.1102A=	XP_005262454.1:p.Ser368=
XM_005262397.4:c.1102A=	XP_005262454.1:p.Ser368=