Canonical Allele Identifier: CA343128605
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552651T>A , CM000663.2:g.169552651T>A GRCh38
NC_000001.10:g.169521889T>A , CM000663.1:g.169521889T>A GRCh37
NC_000001.9:g.167788513T>A NCBI36
NG_011806.1:g.38881A>T , LRG_553:g.38881A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1202A>T MANE Select ENSP00000356771.3:p.Asp401Val
ENST00000367796.3:c.1202A>T ENSP00000356770.3:p.Asp401Val
ENST00000367797.7:c.1202A>T ENSP00000356771.3:p.Asp401Val
NM_000130.4:c.1202A>T , LRG_553t1:c.1202A>T NP_000121.2:p.Asp401Val
XM_017000660.2:c.791A>T XP_016856149.1:p.Asp264Val
NM_000130.5:c.1202A>T MANE Select NP_000121.2:p.Asp401Val