Canonical Allele Identifier: CA343118697
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541806G>A , CM000663.2:g.169541806G>A GRCh38
NC_000001.10:g.169511044G>A , CM000663.1:g.169511044G>A GRCh37
NC_000001.9:g.167777668G>A NCBI36
NG_011806.1:g.49726C>T , LRG_553:g.49726C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.3284C>T MANE Select ENSP00000356771.3:p.Ala1095Val
ENST00000367796.3:c.3299C>T ENSP00000356770.3:p.Ala1100Val
ENST00000367797.7:c.3284C>T ENSP00000356771.3:p.Ala1095Val
NM_000130.4:c.3284C>T , LRG_553t1:c.3284C>T NP_000121.2:p.Ala1095Val
XM_017000660.2:c.2873C>T XP_016856149.1:p.Ala958Val
NM_000130.5:c.3284C>T MANE Select NP_000121.2:p.Ala1095Val