Canonical Allele Identifier: CA2649036591

Gene: F5

Linked Data

• gnomAD v4: 1-169572198-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572203dup , CM000663.2:g.169572203dup	GRCh38
NC_000001.10:g.169541441dup , CM000663.1:g.169541441dup	GRCh37
NC_000001.9:g.167808065dup	NCBI36
NG_011806.1:g.19333dup , LRG_553:g.19333dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.373+22dup MANE Select	ENSP00000356771.3:n.373+22dup
ENST00000367796.3:c.373+22dup	ENSP00000356770.3:n.373+22dup
ENST00000367797.7:c.373+22dup	ENSP00000356771.3:n.373+22dup
NM_000130.4:c.373+22dup , LRG_553t1:c.373+22dup	NP_000121.2:n.373+22dup
XM_017000660.2:c.-39+22dup	XP_016856149.1:n.-39+22dup
NM_000130.5:c.373+22dup MANE Select	NP_000121.2:n.373+22dup