Canonical Allele Identifier: CA2649035845

Gene: F5

Linked Data

• gnomAD v4: 1-169530729-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169530731del , CM000663.2:g.169530731del	GRCh38
NC_000001.10:g.169499969del , CM000663.1:g.169499969del	GRCh37
NC_000001.9:g.167766593del	NCBI36
NG_011806.1:g.60802del , LRG_553:g.60802del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5208+56del MANE Select	ENSP00000356771.3:n.5208+56del
ENST00000367796.3:c.5223+56del	ENSP00000356770.3:n.5223+56del
ENST00000367797.7:c.5208+56del	ENSP00000356771.3:n.5208+56del
NM_000130.4:c.5208+56del , LRG_553t1:c.5208+56del	NP_000121.2:n.5208+56del
XM_017000660.2:c.4797+56del	XP_016856149.1:n.4797+56del
NM_000130.5:c.5208+56del MANE Select	NP_000121.2:n.5208+56del