Canonical Allele Identifier: CA1144493846
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169529742A= , CM000663.2:g.169529742A= GRCh38
NC_000001.10:g.169498980A= , CM000663.1:g.169498980A= GRCh37
NC_000001.9:g.167765604A= NCBI36
NG_011806.1:g.61790T= , LRG_553:g.61790T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5285T= MANE Select ENSP00000356771.3:p.Met1762=
ENST00000367796.3:c.5300T= ENSP00000356770.3:p.Met1767=
ENST00000367797.7:c.5285T= ENSP00000356771.3:p.Met1762=
NM_000130.4:c.5285T= , LRG_553t1:c.5285T= NP_000121.2:p.Met1762=
XM_017000660.2:c.4874T= XP_016856149.1:p.Met1625=
NM_000130.5:c.5285T= MANE Select NP_000121.2:p.Met1762=