Canonical Allele Identifier: CA1206149037

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555013T= , CM000663.2:g.169555013T=	GRCh38
NC_000001.10:g.169524251T= , CM000663.1:g.169524251T=	GRCh37
NC_000001.9:g.167790875T=	NCBI36
NG_011806.1:g.36519A= , LRG_553:g.36519A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+169A= MANE Select	ENSP00000356771.3:n.1118+169A=
ENST00000367796.3:c.1118+169A=	ENSP00000356770.3:n.1118+169A=
ENST00000367797.7:c.1118+169A=	ENSP00000356771.3:n.1118+169A=
NM_000130.4:c.1118+169A= , LRG_553t1:c.1118+169A=	NP_000121.2:n.1118+169A=
XM_017000660.2:c.707+169A=	XP_016856149.1:n.707+169A=
NM_000130.5:c.1118+169A= MANE Select	NP_000121.2:n.1118+169A=