Canonical Allele Identifier: CA1206149457
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555378C= , CM000663.2:g.169555378C= GRCh38
NC_000001.10:g.169524616C= , CM000663.1:g.169524616C= GRCh37
NC_000001.9:g.167791240C= NCBI36
NG_011806.1:g.36154G= , LRG_553:g.36154G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.953-31G= MANE Select ENSP00000356771.3:n.953-31G=
ENST00000367796.3:c.953-31G= ENSP00000356770.3:n.953-31G=
ENST00000367797.7:c.953-31G= ENSP00000356771.3:n.953-31G=
NM_000130.4:c.953-31G= , LRG_553t1:c.953-31G= NP_000121.2:n.953-31G=
XM_017000660.2:c.542-31G= XP_016856149.1:n.542-31G=
NM_000130.5:c.953-31G= MANE Select NP_000121.2:n.953-31G=