Canonical Allele Identifier: CA343128567
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552643A>T , CM000663.2:g.169552643A>T GRCh38
NC_000001.10:g.169521881A>T , CM000663.1:g.169521881A>T GRCh37
NC_000001.9:g.167788505A>T NCBI36
NG_011806.1:g.38889T>A , LRG_553:g.38889T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1210T>A MANE Select ENSP00000356771.3:p.Phe404Ile
ENST00000367796.3:c.1210T>A ENSP00000356770.3:p.Phe404Ile
ENST00000367797.7:c.1210T>A ENSP00000356771.3:p.Phe404Ile
NM_000130.4:c.1210T>A , LRG_553t1:c.1210T>A NP_000121.2:p.Phe404Ile
XM_017000660.2:c.799T>A XP_016856149.1:p.Phe267Ile
NM_000130.5:c.1210T>A MANE Select NP_000121.2:p.Phe404Ile