Canonical Allele Identifier: CA1206135836
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169529744G= , CM000663.2:g.169529744G= GRCh38
NC_000001.10:g.169498982G= , CM000663.1:g.169498982G= GRCh37
NC_000001.9:g.167765606G= NCBI36
NG_011806.1:g.61788C= , LRG_553:g.61788C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5283C= MANE Select ENSP00000356771.3:p.Asn1761=
ENST00000367796.3:c.5298C= ENSP00000356770.3:p.Asn1766=
ENST00000367797.7:c.5283C= ENSP00000356771.3:p.Asn1761=
NM_000130.4:c.5283C= , LRG_553t1:c.5283C= NP_000121.2:p.Asn1761=
XM_017000660.2:c.4872C= XP_016856149.1:p.Asn1624=
NM_000130.5:c.5283C= MANE Select NP_000121.2:p.Asn1761=