Canonical Allele Identifier: CA2466857758

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996984T= , CM000685.2:g.154996984T=	GRCh38
NC_000023.10:g.154225259T= , CM000685.1:g.154225259T=	GRCh37
NC_000023.9:g.153878453T=	NCBI36
NG_011403.1:g.30740A=
NG_011403.2:g.30740A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.377A= MANE Select	ENSP00000353393.4:p.Lys126=
ENST00000647125.1:c.*163A=	ENSP00000496062.1:n.*163A=
ENST00000360256.8:c.377A=	ENSP00000353393.4:p.Lys126=
ENST00000423959.5:c.272A=	ENSP00000409446.1:p.Lys91=
ENST00000453950.1:c.359A=	ENSP00000389153.1:p.Lys120=
NM_000132.3:c.377A=	NP_000123.1:p.Lys126=
XM_011531126.1:c.272A=	XP_011529428.1:p.Lys91=
NM_000132.4:c.377A= MANE Select	NP_000123.1:p.Lys126=