Canonical Allele Identifier: CA1008977085

Gene: F5

Linked Data

• gnomAD v3: 1-169549629-C-CA
• gnomAD v4: 1-169549629-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549631dup , CM000663.2:g.169549631dup	GRCh38
NC_000001.10:g.169518869dup , CM000663.1:g.169518869dup	GRCh37
NC_000001.9:g.167785493dup	NCBI36
NG_011806.1:g.41902dup , LRG_553:g.41902dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1611+171dup MANE Select	ENSP00000356771.3:n.1611+171dup
ENST00000367796.3:c.1611+171dup	ENSP00000356770.3:n.1611+171dup
ENST00000367797.7:c.1611+171dup	ENSP00000356771.3:n.1611+171dup
NM_000130.4:c.1611+171dup , LRG_553t1:c.1611+171dup	NP_000121.2:n.1611+171dup
XM_017000660.2:c.1200+171dup	XP_016856149.1:n.1200+171dup
NM_000130.5:c.1611+171dup MANE Select	NP_000121.2:n.1611+171dup