Canonical Allele Identifier: CA1206132464
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541819A= , CM000663.2:g.169541819A= GRCh38
NC_000001.10:g.169511057A= , CM000663.1:g.169511057A= GRCh37
NC_000001.9:g.167777681A= NCBI36
NG_011806.1:g.49713T= , LRG_553:g.49713T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.3271T= MANE Select ENSP00000356771.3:p.Phe1091=
ENST00000367796.3:c.3286T= ENSP00000356770.3:p.Phe1096=
ENST00000367797.7:c.3271T= ENSP00000356771.3:p.Phe1091=
NM_000130.4:c.3271T= , LRG_553t1:c.3271T= NP_000121.2:p.Phe1091=
XM_017000660.2:c.2860T= XP_016856149.1:p.Phe954=
NM_000130.5:c.3271T= MANE Select NP_000121.2:p.Phe1091=