Canonical Allele Identifier: CA1206136770

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532393_169532394delinsAG , CM000663.2:g.169532393_169532394delinsAG	GRCh38
NC_000001.10:g.169501631_169501632delinsAG , CM000663.1:g.169501631_169501632delinsAG	GRCh37
NC_000001.9:g.167768255_167768256delinsAG	NCBI36
NG_011806.1:g.59138_59139delinsCT , LRG_553:g.59138_59139delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.4972-1372_4972-1371delinsCT MANE Select	ENSP00000356771.3:n.4972-1372_4972-1371delinsCT
ENST00000367796.3:c.4987-1372_4987-1371delinsCT	ENSP00000356770.3:n.4987-1372_4987-1371delinsCT
ENST00000367797.7:c.4972-1372_4972-1371delinsCT	ENSP00000356771.3:n.4972-1372_4972-1371delinsCT
NM_000130.4:c.4972-1372_4972-1371delinsCT , LRG_553t1:c.4972-1372_4972-1371delinsCT	NP_000121.2:n.4972-1372_4972-1371delinsCT
XM_017000660.2:c.4561-1372_4561-1371delinsCT	XP_016856149.1:n.4561-1372_4561-1371delinsCT
NM_000130.5:c.4972-1372_4972-1371delinsCT MANE Select	NP_000121.2:n.4972-1372_4972-1371delinsCT