Canonical Allele Identifier: CA2554684548

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169554883_169554884insGCAAATTAAACTTCATGGG , CM000663.2:g.169554883_169554884insGCAAATTAAACTTCATGGG	GRCh38
NC_000001.10:g.169524121_169524122insGCAAATTAAACTTCATGGG , CM000663.1:g.169524121_169524122insGCAAATTAAACTTCATGGG	GRCh37
NC_000001.9:g.167790745_167790746insGCAAATTAAACTTCATGGG	NCBI36
NG_011806.1:g.36648_36649insCCCATGAAGTTTAATTTGC , LRG_553:g.36648_36649insCCCATGAAGTTTAATTTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+298_1118+299insCCCATGAAGTTTAATTTGC MANE Select	ENSP00000356771.3:n.1118+298_1118+299insCCCATGAAGTTTAATTTGC
ENST00000367796.3:c.1118+298_1118+299insCCCATGAAGTTTAATTTGC	ENSP00000356770.3:n.1118+298_1118+299insCCCATGAAGTTTAATTTGC
ENST00000367797.7:c.1118+298_1118+299insCCCATGAAGTTTAATTTGC	ENSP00000356771.3:n.1118+298_1118+299insCCCATGAAGTTTAATTTGC
NM_000130.4:c.1118+298_1118+299insCCCATGAAGTTTAATTTGC , LRG_553t1:c.1118+298_1118+299insCCCATGAAGTTTAATTTGC	NP_000121.2:n.1118+298_1118+299insCCCATGAAGTTTAATTTGC
XM_017000660.2:c.707+298_707+299insCCCATGAAGTTTAATTTGC	XP_016856149.1:n.707+298_707+299insCCCATGAAGTTTAATTTGC
NM_000130.5:c.1118+298_1118+299insCCCATGAAGTTTAATTTGC MANE Select	NP_000121.2:n.1118+298_1118+299insCCCATGAAGTTTAATTTGC