Canonical Allele Identifier: CA2547831561

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572207del , CM000663.2:g.169572207del	GRCh38
NC_000001.10:g.169541445del , CM000663.1:g.169541445del	GRCh37
NC_000001.9:g.167808069del	NCBI36
NG_011806.1:g.19326del , LRG_553:g.19326del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.373+15del MANE Select	ENSP00000356771.3:n.373+15del
ENST00000367796.3:c.373+15del	ENSP00000356770.3:n.373+15del
ENST00000367797.7:c.373+15del	ENSP00000356771.3:n.373+15del
NM_000130.4:c.373+15del , LRG_553t1:c.373+15del	NP_000121.2:n.373+15del
XM_017000660.2:c.-39+15del	XP_016856149.1:n.-39+15del
NM_000130.5:c.373+15del MANE Select	NP_000121.2:n.373+15del