Canonical Allele Identifier: CA1206148908

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169554856_169554857delinsAC , CM000663.2:g.169554856_169554857delinsAC	GRCh38
NC_000001.10:g.169524094_169524095delinsAC , CM000663.1:g.169524094_169524095delinsAC	GRCh37
NC_000001.9:g.167790718_167790719delinsAC	NCBI36
NG_011806.1:g.36675_36676delinsGT , LRG_553:g.36675_36676delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+325_1118+326delinsGT MANE Select	ENSP00000356771.3:n.1118+325_1118+326delinsGT
ENST00000367796.3:c.1118+325_1118+326delinsGT	ENSP00000356770.3:n.1118+325_1118+326delinsGT
ENST00000367797.7:c.1118+325_1118+326delinsGT	ENSP00000356771.3:n.1118+325_1118+326delinsGT
NM_000130.4:c.1118+325_1118+326delinsGT , LRG_553t1:c.1118+325_1118+326delinsGT	NP_000121.2:n.1118+325_1118+326delinsGT
XM_017000660.2:c.707+325_707+326delinsGT	XP_016856149.1:n.707+325_707+326delinsGT
NM_000130.5:c.1118+325_1118+326delinsGT MANE Select	NP_000121.2:n.1118+325_1118+326delinsGT