Canonical Allele Identifier: CA1144229039
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525949C= , CM000663.2:g.169525949C= GRCh38
NC_000001.10:g.169495187C= , CM000663.1:g.169495187C= GRCh37
NC_000001.9:g.167761811C= NCBI36
NG_011806.1:g.65583G= , LRG_553:g.65583G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5668G= MANE Select ENSP00000356771.3:p.Glu1890=
ENST00000367796.3:c.5683G= ENSP00000356770.3:p.Glu1895=
ENST00000367797.7:c.5668G= ENSP00000356771.3:p.Glu1890=
NM_000130.4:c.5668G= , LRG_553t1:c.5668G= NP_000121.2:p.Glu1890=
XM_017000660.2:c.5257G= XP_016856149.1:p.Glu1753=
NM_000130.5:c.5668G= MANE Select NP_000121.2:p.Glu1890=