Canonical Allele Identifier: CA1206144046

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549633_169549634delinsAC , CM000663.2:g.169549633_169549634delinsAC	GRCh38
NC_000001.10:g.169518871_169518872delinsAC , CM000663.1:g.169518871_169518872delinsAC	GRCh37
NC_000001.9:g.167785495_167785496delinsAC	NCBI36
NG_011806.1:g.41898_41899delinsGT , LRG_553:g.41898_41899delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.1611+167_1611+168delinsGT MANE Select	ENSP00000356771.3:n.1611+167_1611+168delinsGT
ENST00000367796.3:c.1611+167_1611+168delinsGT	ENSP00000356770.3:n.1611+167_1611+168delinsGT
ENST00000367797.7:c.1611+167_1611+168delinsGT	ENSP00000356771.3:n.1611+167_1611+168delinsGT
NM_000130.4:c.1611+167_1611+168delinsGT , LRG_553t1:c.1611+167_1611+168delinsGT	NP_000121.2:n.1611+167_1611+168delinsGT
XM_017000660.2:c.1200+167_1200+168delinsGT	XP_016856149.1:n.1200+167_1200+168delinsGT
NM_000130.5:c.1611+167_1611+168delinsGT MANE Select	NP_000121.2:n.1611+167_1611+168delinsGT