Canonical Allele Identifier: CA1206136768

Gene: F5

Linked Data

• dbSNP Id: rs1659610578

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532385del , CM000663.2:g.169532385del	GRCh38
NC_000001.10:g.169501623del , CM000663.1:g.169501623del	GRCh37
NC_000001.9:g.167768247del	NCBI36
NG_011806.1:g.59149del , LRG_553:g.59149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.4972-1361del MANE Select	ENSP00000356771.3:n.4972-1361del
ENST00000367796.3:c.4987-1361del	ENSP00000356770.3:n.4987-1361del
ENST00000367797.7:c.4972-1361del	ENSP00000356771.3:n.4972-1361del
NM_000130.4:c.4972-1361del , LRG_553t1:c.4972-1361del	NP_000121.2:n.4972-1361del
XM_017000660.2:c.4561-1361del	XP_016856149.1:n.4561-1361del
NM_000130.5:c.4972-1361del MANE Select	NP_000121.2:n.4972-1361del