Canonical Allele Identifier: CA1147832150

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555314C= , CM000663.2:g.169555314C=	GRCh38
NC_000001.10:g.169524552C= , CM000663.1:g.169524552C=	GRCh37
NC_000001.9:g.167791176C=	NCBI36
NG_011806.1:g.36218G= , LRG_553:g.36218G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.986G= MANE Select	ENSP00000356771.3:p.Cys329=
ENST00000367796.3:c.986G=	ENSP00000356770.3:p.Cys329=
ENST00000367797.7:c.986G=	ENSP00000356771.3:p.Cys329=
NM_000130.4:c.986G= , LRG_553t1:c.986G=	NP_000121.2:p.Cys329=
XM_017000660.2:c.575G=	XP_016856149.1:p.Cys192=
NM_000130.5:c.986G= MANE Select	NP_000121.2:p.Cys329=