Canonical Allele Identifier: CA1206132462
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541815C= , CM000663.2:g.169541815C= GRCh38
NC_000001.10:g.169511053C= , CM000663.1:g.169511053C= GRCh37
NC_000001.9:g.167777677C= NCBI36
NG_011806.1:g.49717G= , LRG_553:g.49717G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.3275G= MANE Select ENSP00000356771.3:p.Gly1092=
ENST00000367796.3:c.3290G= ENSP00000356770.3:p.Gly1097=
ENST00000367797.7:c.3275G= ENSP00000356771.3:p.Gly1092=
NM_000130.4:c.3275G= , LRG_553t1:c.3275G= NP_000121.2:p.Gly1092=
XM_017000660.2:c.2864G= XP_016856149.1:p.Gly955=
NM_000130.5:c.3275G= MANE Select NP_000121.2:p.Gly1092=