Canonical Allele Identifier: CA1206148629

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572268G= , CM000663.2:g.169572268G=	GRCh38
NC_000001.10:g.169541506G= , CM000663.1:g.169541506G=	GRCh37
NC_000001.9:g.167808130G=	NCBI36
NG_011806.1:g.19264C= , LRG_553:g.19264C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.326C= MANE Select	ENSP00000356771.3:p.Pro109=
ENST00000367796.3:c.326C=	ENSP00000356770.3:p.Pro109=
ENST00000367797.7:c.326C=	ENSP00000356771.3:p.Pro109=
NM_000130.4:c.326C= , LRG_553t1:c.326C=	NP_000121.2:p.Pro109=
XM_017000660.2:c.-86C=	XP_016856149.1:n.-86C=
NM_000130.5:c.326C= MANE Select	NP_000121.2:p.Pro109=