Canonical Allele Identifier: CA1206146642

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552400G= , CM000663.2:g.169552400G=	GRCh38
NC_000001.10:g.169521638G= , CM000663.1:g.169521638G=	GRCh37
NC_000001.9:g.167788262G=	NCBI36
NG_011806.1:g.39132C= , LRG_553:g.39132C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1296+157C= MANE Select	ENSP00000356771.3:n.1296+157C=
ENST00000367796.3:c.1296+157C=	ENSP00000356770.3:n.1296+157C=
ENST00000367797.7:c.1296+157C=	ENSP00000356771.3:n.1296+157C=
NM_000130.4:c.1296+157C= , LRG_553t1:c.1296+157C=	NP_000121.2:n.1296+157C=
XM_017000660.2:c.885+157C=	XP_016856149.1:n.885+157C=
NM_000130.5:c.1296+157C= MANE Select	NP_000121.2:n.1296+157C=