Canonical Allele Identifier: CA1206149368
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555307C= , CM000663.2:g.169555307C= GRCh38
NC_000001.10:g.169524545C= , CM000663.1:g.169524545C= GRCh37
NC_000001.9:g.167791169C= NCBI36
NG_011806.1:g.36225G= , LRG_553:g.36225G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.993G= MANE Select ENSP00000356771.3:p.Lys331=
ENST00000367796.3:c.993G= ENSP00000356770.3:p.Lys331=
ENST00000367797.7:c.993G= ENSP00000356771.3:p.Lys331=
NM_000130.4:c.993G= , LRG_553t1:c.993G= NP_000121.2:p.Lys331=
XM_017000660.2:c.582G= XP_016856149.1:p.Lys194=
NM_000130.5:c.993G= MANE Select NP_000121.2:p.Lys331=