Canonical Allele Identifier: CA1206133732

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169526017C= , CM000663.2:g.169526017C=	GRCh38
NC_000001.10:g.169495255C= , CM000663.1:g.169495255C=	GRCh37
NC_000001.9:g.167761879C=	NCBI36
NG_011806.1:g.65515G= , LRG_553:g.65515G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5600G= MANE Select	ENSP00000356771.3:p.Gly1867=
ENST00000367796.3:c.5615G=	ENSP00000356770.3:p.Gly1872=
ENST00000367797.7:c.5600G=	ENSP00000356771.3:p.Gly1867=
NM_000130.4:c.5600G= , LRG_553t1:c.5600G=	NP_000121.2:p.Gly1867=
XM_017000660.2:c.5189G=	XP_016856149.1:p.Gly1730=
NM_000130.5:c.5600G= MANE Select	NP_000121.2:p.Gly1867=