Canonical Allele Identifier: CA343128704
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552664T>A , CM000663.2:g.169552664T>A GRCh38
NC_000001.10:g.169521902T>A , CM000663.1:g.169521902T>A GRCh37
NC_000001.9:g.167788526T>A NCBI36
NG_011806.1:g.38868A>T , LRG_553:g.38868A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1189A>T MANE Select ENSP00000356771.3:p.Thr397Ser
ENST00000367796.3:c.1189A>T ENSP00000356770.3:p.Thr397Ser
ENST00000367797.7:c.1189A>T ENSP00000356771.3:p.Thr397Ser
NM_000130.4:c.1189A>T , LRG_553t1:c.1189A>T NP_000121.2:p.Thr397Ser
XM_017000660.2:c.778A>T XP_016856149.1:p.Thr260Ser
NM_000130.5:c.1189A>T MANE Select NP_000121.2:p.Thr397Ser