Canonical Allele Identifier: CA343131279
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555236G>A , CM000663.2:g.169555236G>A GRCh38
NC_000001.10:g.169524474G>A , CM000663.1:g.169524474G>A GRCh37
NC_000001.9:g.167791098G>A NCBI36
NG_011806.1:g.36296C>T , LRG_553:g.36296C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1064C>T MANE Select ENSP00000356771.3:p.Ala355Val
ENST00000367796.3:c.1064C>T ENSP00000356770.3:p.Ala355Val
ENST00000367797.7:c.1064C>T ENSP00000356771.3:p.Ala355Val
NM_000130.4:c.1064C>T , LRG_553t1:c.1064C>T NP_000121.2:p.Ala355Val
XM_017000660.2:c.653C>T XP_016856149.1:p.Ala218Val
NM_000130.5:c.1064C>T MANE Select NP_000121.2:p.Ala355Val