Canonical Allele Identifier: CA2649037751
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586500del , CM000663.2:g.169586500del GRCh38
NC_000001.10:g.169555738del , CM000663.1:g.169555738del GRCh37
NC_000001.9:g.167822362del NCBI36
NG_011806.1:g.5034del , LRG_553:g.5034del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-112del ENSP00000356770.3:n.-112del
ENST00000367797.7:c.-112del ENSP00000356771.3:n.-112del
NM_000130.4:c.-112del , LRG_553t1:c.-112del NP_000121.2:n.-112del
XM_017000660.2:c.-431del XP_016856149.1:n.-431del