Canonical Allele Identifier: CA1206136759

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532363_169532364delinsGA , CM000663.2:g.169532363_169532364delinsGA	GRCh38
NC_000001.10:g.169501601_169501602delinsGA , CM000663.1:g.169501601_169501602delinsGA	GRCh37
NC_000001.9:g.167768225_167768226delinsGA	NCBI36
NG_011806.1:g.59168_59169delinsTC , LRG_553:g.59168_59169delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.4972-1342_4972-1341delinsTC MANE Select	ENSP00000356771.3:n.4972-1342_4972-1341delinsTC
ENST00000367796.3:c.4987-1342_4987-1341delinsTC	ENSP00000356770.3:n.4987-1342_4987-1341delinsTC
ENST00000367797.7:c.4972-1342_4972-1341delinsTC	ENSP00000356771.3:n.4972-1342_4972-1341delinsTC
NM_000130.4:c.4972-1342_4972-1341delinsTC , LRG_553t1:c.4972-1342_4972-1341delinsTC	NP_000121.2:n.4972-1342_4972-1341delinsTC
XM_017000660.2:c.4561-1342_4561-1341delinsTC	XP_016856149.1:n.4561-1342_4561-1341delinsTC
NM_000130.5:c.4972-1342_4972-1341delinsTC MANE Select	NP_000121.2:n.4972-1342_4972-1341delinsTC