Canonical Allele Identifier: CA1206147010
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552749_169552762delinsAAAAAAAATTAAAC , CM000663.2:g.169552749_169552762delinsAAAAAAAATTAAAC GRCh38
NC_000001.10:g.169521987_169522000delinsAAAAAAAATTAAAC , CM000663.1:g.169521987_169522000delinsAAAAAAAATTAAAC GRCh37
NC_000001.9:g.167788611_167788624delinsAAAAAAAATTAAAC NCBI36
NG_011806.1:g.38770_38783delinsGTTTAATTTTTTTT , LRG_553:g.38770_38783delinsGTTTAATTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1119-28_1119-15delinsGTTTAATTTTTTTT MANE Select ENSP00000356771.3:n.1119-28_1119-15delinsGTTTAATTTTTTTT
ENST00000367796.3:c.1119-28_1119-15delinsGTTTAATTTTTTTT ENSP00000356770.3:n.1119-28_1119-15delinsGTTTAATTTTTTTT
ENST00000367797.7:c.1119-28_1119-15delinsGTTTAATTTTTTTT ENSP00000356771.3:n.1119-28_1119-15delinsGTTTAATTTTTTTT
NM_000130.4:c.1119-28_1119-15delinsGTTTAATTTTTTTT , LRG_553t1:c.1119-28_1119-15delinsGTTTAATTTTTTTT NP_000121.2:n.1119-28_1119-15delinsGTTTAATTTTTTTT
XM_017000660.2:c.708-28_708-15delinsGTTTAATTTTTTTT XP_016856149.1:n.708-28_708-15delinsGTTTAATTTTTTTT
NM_000130.5:c.1119-28_1119-15delinsGTTTAATTTTTTTT MANE Select NP_000121.2:n.1119-28_1119-15delinsGTTTAATTTTTTTT