Canonical Allele Identifier: CA1206144025

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549626_169549627delinsAG , CM000663.2:g.169549626_169549627delinsAG	GRCh38
NC_000001.10:g.169518864_169518865delinsAG , CM000663.1:g.169518864_169518865delinsAG	GRCh37
NC_000001.9:g.167785488_167785489delinsAG	NCBI36
NG_011806.1:g.41905_41906delinsCT , LRG_553:g.41905_41906delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.1611+174_1611+175delinsCT MANE Select	ENSP00000356771.3:n.1611+174_1611+175delinsCT
ENST00000367796.3:c.1611+174_1611+175delinsCT	ENSP00000356770.3:n.1611+174_1611+175delinsCT
ENST00000367797.7:c.1611+174_1611+175delinsCT	ENSP00000356771.3:n.1611+174_1611+175delinsCT
NM_000130.4:c.1611+174_1611+175delinsCT , LRG_553t1:c.1611+174_1611+175delinsCT	NP_000121.2:n.1611+174_1611+175delinsCT
XM_017000660.2:c.1200+174_1200+175delinsCT	XP_016856149.1:n.1200+174_1200+175delinsCT
NM_000130.5:c.1611+174_1611+175delinsCT MANE Select	NP_000121.2:n.1611+174_1611+175delinsCT