Canonical Allele Identifier: CA1139773084
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169529737T= , CM000663.2:g.169529737T= GRCh38
NC_000001.10:g.169498975T= , CM000663.1:g.169498975T= GRCh37
NC_000001.9:g.167765599T= NCBI36
NG_011806.1:g.61795A= , LRG_553:g.61795A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5290A= MANE Select ENSP00000356771.3:p.Met1764=
ENST00000367796.3:c.5305A= ENSP00000356770.3:p.Met1769=
ENST00000367797.7:c.5290A= ENSP00000356771.3:p.Met1764=
NM_000130.4:c.5290A= , LRG_553t1:c.5290A= NP_000121.2:p.Met1764=
XM_017000660.2:c.4879A= XP_016856149.1:p.Met1627=
NM_000130.5:c.5290A= MANE Select NP_000121.2:p.Met1764=