Canonical Allele Identifier: CA1206136762

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532373A= , CM000663.2:g.169532373A=	GRCh38
NC_000001.10:g.169501611A= , CM000663.1:g.169501611A=	GRCh37
NC_000001.9:g.167768235A=	NCBI36
NG_011806.1:g.59159T= , LRG_553:g.59159T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.4972-1351T= MANE Select	ENSP00000356771.3:n.4972-1351T=
ENST00000367796.3:c.4987-1351T=	ENSP00000356770.3:n.4987-1351T=
ENST00000367797.7:c.4972-1351T=	ENSP00000356771.3:n.4972-1351T=
NM_000130.4:c.4972-1351T= , LRG_553t1:c.4972-1351T=	NP_000121.2:n.4972-1351T=
XM_017000660.2:c.4561-1351T=	XP_016856149.1:n.4561-1351T=
NM_000130.5:c.4972-1351T= MANE Select	NP_000121.2:n.4972-1351T=