Canonical Allele Identifier: CA1206136160

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169530627C= , CM000663.2:g.169530627C=	GRCh38
NC_000001.10:g.169499865C= , CM000663.1:g.169499865C=	GRCh37
NC_000001.9:g.167766489C=	NCBI36
NG_011806.1:g.60905G= , LRG_553:g.60905G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5208+159G= MANE Select	ENSP00000356771.3:n.5208+159G=
ENST00000367796.3:c.5223+159G=	ENSP00000356770.3:n.5223+159G=
ENST00000367797.7:c.5208+159G=	ENSP00000356771.3:n.5208+159G=
NM_000130.4:c.5208+159G= , LRG_553t1:c.5208+159G=	NP_000121.2:n.5208+159G=
XM_017000660.2:c.4797+159G=	XP_016856149.1:n.4797+159G=
NM_000130.5:c.5208+159G= MANE Select	NP_000121.2:n.5208+159G=