Canonical Allele Identifier: CA2466856576

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993143C= , CM000685.2:g.154993143C=	GRCh38
NC_000023.10:g.154221418C= , CM000685.1:g.154221418C=	GRCh37
NC_000023.9:g.153874612C=	NCBI36
NG_011403.1:g.34581G=
NG_011403.2:g.34581G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.394G= MANE Select	ENSP00000353393.4:p.Glu132=
ENST00000647125.1:c.*180G=	ENSP00000496062.1:n.*180G=
ENST00000360256.8:c.394G=	ENSP00000353393.4:p.Glu132=
ENST00000423959.5:c.289G=	ENSP00000409446.1:p.Glu97=
ENST00000453950.1:c.376G=	ENSP00000389153.1:p.Glu126=
NM_000132.3:c.394G=	NP_000123.1:p.Glu132=
XM_011531126.1:c.289G=	XP_011529428.1:p.Glu97=
NM_000132.4:c.394G= MANE Select	NP_000123.1:p.Glu132=