Canonical Allele Identifier: CA2649036753

Gene: F5

Linked Data

• gnomAD v4: 1-169572287-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572290del , CM000663.2:g.169572290del	GRCh38
NC_000001.10:g.169541528del , CM000663.1:g.169541528del	GRCh37
NC_000001.9:g.167808152del	NCBI36
NG_011806.1:g.19244del , LRG_553:g.19244del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.306del MANE Select	ENSP00000356771.3:p.Phe102LeufsTer9
ENST00000367796.3:c.306del	ENSP00000356770.3:p.Phe102LeufsTer9
ENST00000367797.7:c.306del	ENSP00000356771.3:p.Phe102LeufsTer9
NM_000130.4:c.306del , LRG_553t1:c.306del	NP_000121.2:p.Phe102LeufsTer9
XM_017000660.2:c.-106del	XP_016856149.1:n.-106del
NM_000130.5:c.306del MANE Select	NP_000121.2:p.Phe102LeufsTer9