Canonical Allele Identifier: CA1206136766

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532381C= , CM000663.2:g.169532381C=	GRCh38
NC_000001.10:g.169501619C= , CM000663.1:g.169501619C=	GRCh37
NC_000001.9:g.167768243C=	NCBI36
NG_011806.1:g.59151G= , LRG_553:g.59151G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.4972-1359G= MANE Select	ENSP00000356771.3:n.4972-1359G=
ENST00000367796.3:c.4987-1359G=	ENSP00000356770.3:n.4987-1359G=
ENST00000367797.7:c.4972-1359G=	ENSP00000356771.3:n.4972-1359G=
NM_000130.4:c.4972-1359G= , LRG_553t1:c.4972-1359G=	NP_000121.2:n.4972-1359G=
XM_017000660.2:c.4561-1359G=	XP_016856149.1:n.4561-1359G=
NM_000130.5:c.4972-1359G= MANE Select	NP_000121.2:n.4972-1359G=