Canonical Allele Identifier: CA1206146897

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552661G= , CM000663.2:g.169552661G=	GRCh38
NC_000001.10:g.169521899G= , CM000663.1:g.169521899G=	GRCh37
NC_000001.9:g.167788523G=	NCBI36
NG_011806.1:g.38871C= , LRG_553:g.38871C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1192C= MANE Select	ENSP00000356771.3:p.Gln398=
ENST00000367796.3:c.1192C=	ENSP00000356770.3:p.Gln398=
ENST00000367797.7:c.1192C=	ENSP00000356771.3:p.Gln398=
NM_000130.4:c.1192C= , LRG_553t1:c.1192C=	NP_000121.2:p.Gln398=
XM_017000660.2:c.781C=	XP_016856149.1:p.Gln261=
NM_000130.5:c.1192C= MANE Select	NP_000121.2:p.Gln398=