Canonical Allele Identifier: CA890930145

Gene: F5

Linked Data

• dbSNP Id: rs1361220293
• gnomAD v4: 1-169555375-TAACTC-T
• MyVariant Identifiers: chr1:g.169524614_169524618del (hg19) ; chr1:g.169555376_169555380del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555378_169555382del , CM000663.2:g.169555378_169555382del	GRCh38
NC_000001.10:g.169524616_169524620del , CM000663.1:g.169524616_169524620del	GRCh37
NC_000001.9:g.167791240_167791244del	NCBI36
NG_011806.1:g.36152_36156del , LRG_553:g.36152_36156del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.953-33_953-29del MANE Select	ENSP00000356771.3:n.953-33_953-29del
ENST00000367796.3:c.953-33_953-29del	ENSP00000356770.3:n.953-33_953-29del
ENST00000367797.7:c.953-33_953-29del	ENSP00000356771.3:n.953-33_953-29del
NM_000130.4:c.953-33_953-29del , LRG_553t1:c.953-33_953-29del	NP_000121.2:n.953-33_953-29del
XM_017000660.2:c.542-33_542-29del	XP_016856149.1:n.542-33_542-29del
NM_000130.5:c.953-33_953-29del MANE Select	NP_000121.2:n.953-33_953-29del