Canonical Allele Identifier: CA1206136767

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532382_169532383delinsCA , CM000663.2:g.169532382_169532383delinsCA	GRCh38
NC_000001.10:g.169501620_169501621delinsCA , CM000663.1:g.169501620_169501621delinsCA	GRCh37
NC_000001.9:g.167768244_167768245delinsCA	NCBI36
NG_011806.1:g.59149_59150delinsTG , LRG_553:g.59149_59150delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.4972-1361_4972-1360delinsTG MANE Select	ENSP00000356771.3:n.4972-1361_4972-1360delinsTG
ENST00000367796.3:c.4987-1361_4987-1360delinsTG	ENSP00000356770.3:n.4987-1361_4987-1360delinsTG
ENST00000367797.7:c.4972-1361_4972-1360delinsTG	ENSP00000356771.3:n.4972-1361_4972-1360delinsTG
NM_000130.4:c.4972-1361_4972-1360delinsTG , LRG_553t1:c.4972-1361_4972-1360delinsTG	NP_000121.2:n.4972-1361_4972-1360delinsTG
XM_017000660.2:c.4561-1361_4561-1360delinsTG	XP_016856149.1:n.4561-1361_4561-1360delinsTG
NM_000130.5:c.4972-1361_4972-1360delinsTG MANE Select	NP_000121.2:n.4972-1361_4972-1360delinsTG