Canonical Allele Identifier: CA2586964382

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541936_169541937insAG , CM000663.2:g.169541936_169541937insAG	GRCh38
NC_000001.10:g.169511174_169511175insAG , CM000663.1:g.169511174_169511175insAG	GRCh37
NC_000001.9:g.167777798_167777799insAG	NCBI36
NG_011806.1:g.49595_49596insCT , LRG_553:g.49595_49596insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3153_3154insCT MANE Select	ENSP00000356771.3:p.Arg1052LeufsTer?
ENST00000367796.3:c.3168_3169insCT	ENSP00000356770.3:p.Arg1057LeufsTer?
ENST00000367797.7:c.3153_3154insCT	ENSP00000356771.3:p.Arg1052LeufsTer?
NM_000130.4:c.3153_3154insCT , LRG_553t1:c.3153_3154insCT	NP_000121.2:p.Arg1052LeufsTer?
XM_017000660.2:c.2742_2743insCT	XP_016856149.1:p.Arg915LeufsTer?
NM_000130.5:c.3153_3154insCT MANE Select	NP_000121.2:p.Arg1052LeufsTer?