Canonical Allele Identifier: CA890924717

Gene: F5

Linked Data

• dbSNP Id: rs1476027658
• gnomAD v3: 1-169532518-T-TACAAAATC
• gnomAD v4: 1-169532518-T-TACAAAATC
• MyVariant Identifiers: chr1:g.169501756_169501757insACAAAATC (hg19) ; chr1:g.169532518_169532519insACAAAATC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532520_169532527dup , CM000663.2:g.169532520_169532527dup	GRCh38
NC_000001.10:g.169501758_169501765dup , CM000663.1:g.169501758_169501765dup	GRCh37
NC_000001.9:g.167768382_167768389dup	NCBI36
NG_011806.1:g.59006_59013dup , LRG_553:g.59006_59013dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.4972-1504_4972-1497dup MANE Select	ENSP00000356771.3:n.4972-1504_4972-1497dup
ENST00000367796.3:c.4987-1504_4987-1497dup	ENSP00000356770.3:n.4987-1504_4987-1497dup
ENST00000367797.7:c.4972-1504_4972-1497dup	ENSP00000356771.3:n.4972-1504_4972-1497dup
NM_000130.4:c.4972-1504_4972-1497dup , LRG_553t1:c.4972-1504_4972-1497dup	NP_000121.2:n.4972-1504_4972-1497dup
XM_017000660.2:c.4561-1504_4561-1497dup	XP_016856149.1:n.4561-1504_4561-1497dup
NM_000130.5:c.4972-1504_4972-1497dup MANE Select	NP_000121.2:n.4972-1504_4972-1497dup