Canonical Allele Identifier: CA1206148541

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572177C= , CM000663.2:g.169572177C=	GRCh38
NC_000001.10:g.169541415C= , CM000663.1:g.169541415C=	GRCh37
NC_000001.9:g.167808039C=	NCBI36
NG_011806.1:g.19355G= , LRG_553:g.19355G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.373+44G= MANE Select	ENSP00000356771.3:n.373+44G=
ENST00000367796.3:c.373+44G=	ENSP00000356770.3:n.373+44G=
ENST00000367797.7:c.373+44G=	ENSP00000356771.3:n.373+44G=
NM_000130.4:c.373+44G= , LRG_553t1:c.373+44G=	NP_000121.2:n.373+44G=
XM_017000660.2:c.-39+44G=	XP_016856149.1:n.-39+44G=
NM_000130.5:c.373+44G= MANE Select	NP_000121.2:n.373+44G=