Canonical Allele Identifier: CA1206149447

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555367C= , CM000663.2:g.169555367C=	GRCh38
NC_000001.10:g.169524605C= , CM000663.1:g.169524605C=	GRCh37
NC_000001.9:g.167791229C=	NCBI36
NG_011806.1:g.36165G= , LRG_553:g.36165G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.953-20G= MANE Select	ENSP00000356771.3:n.953-20G=
ENST00000367796.3:c.953-20G=	ENSP00000356770.3:n.953-20G=
ENST00000367797.7:c.953-20G=	ENSP00000356771.3:n.953-20G=
NM_000130.4:c.953-20G= , LRG_553t1:c.953-20G=	NP_000121.2:n.953-20G=
XM_017000660.2:c.542-20G=	XP_016856149.1:n.542-20G=
NM_000130.5:c.953-20G= MANE Select	NP_000121.2:n.953-20G=