Canonical Allele Identifier: CA2522700299

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572608_169572609insGTTT , CM000663.2:g.169572608_169572609insGTTT	GRCh38
NC_000001.10:g.169541846_169541847insGTTT , CM000663.1:g.169541846_169541847insGTTT	GRCh37
NC_000001.9:g.167808470_167808471insGTTT	NCBI36
NG_011806.1:g.18924_18925insAACA , LRG_553:g.18924_18925insAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.251-265_251-264insAACA MANE Select	ENSP00000356771.3:n.251-265_251-264insAACA
ENST00000367796.3:c.251-265_251-264insAACA	ENSP00000356770.3:n.251-265_251-264insAACA
ENST00000367797.7:c.251-265_251-264insAACA	ENSP00000356771.3:n.251-265_251-264insAACA
NM_000130.4:c.251-265_251-264insAACA , LRG_553t1:c.251-265_251-264insAACA	NP_000121.2:n.251-265_251-264insAACA
XM_017000660.2:c.-161-265_-161-264insAACA	XP_016856149.1:n.-161-265_-161-264insAACA
NM_000130.5:c.251-265_251-264insAACA MANE Select	NP_000121.2:n.251-265_251-264insAACA