Canonical Allele Identifier: CA2461412229

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561899A= , CM000685.2:g.139561899A=	GRCh38
NC_000023.10:g.138644058A= , CM000685.1:g.138644058A=	GRCh37
NC_000023.9:g.138471724A=	NCBI36
NG_007994.1:g.36164A= , LRG_556:g.36164A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1214A= MANE Select	ENSP00000218099.2:p.Asp405=
ENST00000643157.1:n.1723+158A=
ENST00000218099.6:c.1214A=	ENSP00000218099.2:p.Asp405=
ENST00000394090.2:c.1100A=	ENSP00000377650.2:p.Asp367=
NM_000133.3:c.1214A= , LRG_556t1:c.1214A=	NP_000124.1:p.Asp405=
NM_001313913.1:c.1100A=	NP_001300842.1:p.Asp367=
XM_005262397.3:c.1085A=	XP_005262454.1:p.Asp362=
XM_005262397.4:c.1085A=	XP_005262454.1:p.Asp362=
NM_000133.4:c.1214A= MANE Select	NP_000124.1:p.Asp405=
NM_001313913.2:c.1100A=	NP_001300842.1:p.Asp367=