Canonical Allele Identifier: CA1206133700

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525968G= , CM000663.2:g.169525968G=	GRCh38
NC_000001.10:g.169495206G= , CM000663.1:g.169495206G=	GRCh37
NC_000001.9:g.167761830G=	NCBI36
NG_011806.1:g.65564C= , LRG_553:g.65564C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5649C= MANE Select	ENSP00000356771.3:p.Leu1883=
ENST00000367796.3:c.5664C=	ENSP00000356770.3:p.Leu1888=
ENST00000367797.7:c.5649C=	ENSP00000356771.3:p.Leu1883=
NM_000130.4:c.5649C= , LRG_553t1:c.5649C=	NP_000121.2:p.Leu1883=
XM_017000660.2:c.5238C=	XP_016856149.1:p.Leu1746=
NM_000130.5:c.5649C= MANE Select	NP_000121.2:p.Leu1883=