Canonical Allele Identifier: CA2461412216

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561870C= , CM000685.2:g.139561870C=	GRCh38
NC_000023.10:g.138644029C= , CM000685.1:g.138644029C=	GRCh37
NC_000023.9:g.138471695C=	NCBI36
NG_007994.1:g.36135C= , LRG_556:g.36135C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1185C= MANE Select	ENSP00000218099.2:p.Phe395=
ENST00000643157.1:n.1723+129C=
ENST00000218099.6:c.1185C=	ENSP00000218099.2:p.Phe395=
ENST00000394090.2:c.1071C=	ENSP00000377650.2:p.Phe357=
NM_000133.3:c.1185C= , LRG_556t1:c.1185C=	NP_000124.1:p.Phe395=
NM_001313913.1:c.1071C=	NP_001300842.1:p.Phe357=
XM_005262397.3:c.1056C=	XP_005262454.1:p.Phe352=
XM_005262397.4:c.1056C=	XP_005262454.1:p.Phe352=
NM_000133.4:c.1185C= MANE Select	NP_000124.1:p.Phe395=
NM_001313913.2:c.1071C=	NP_001300842.1:p.Phe357=