Canonical Allele Identifier: CA2649036272

Gene: F5

Linked Data

• gnomAD v4: 1-169555110-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555114dup , CM000663.2:g.169555114dup	GRCh38
NC_000001.10:g.169524352dup , CM000663.1:g.169524352dup	GRCh37
NC_000001.9:g.167790976dup	NCBI36
NG_011806.1:g.36421dup , LRG_553:g.36421dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+71dup MANE Select	ENSP00000356771.3:n.1118+71dup
ENST00000367796.3:c.1118+71dup	ENSP00000356770.3:n.1118+71dup
ENST00000367797.7:c.1118+71dup	ENSP00000356771.3:n.1118+71dup
NM_000130.4:c.1118+71dup , LRG_553t1:c.1118+71dup	NP_000121.2:n.1118+71dup
XM_017000660.2:c.707+71dup	XP_016856149.1:n.707+71dup
NM_000130.5:c.1118+71dup MANE Select	NP_000121.2:n.1118+71dup