Canonical Allele Identifier: CA1206146820

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552607_169552608delinsCT , CM000663.2:g.169552607_169552608delinsCT	GRCh38
NC_000001.10:g.169521845_169521846delinsCT , CM000663.1:g.169521845_169521846delinsCT	GRCh37
NC_000001.9:g.167788469_167788470delinsCT	NCBI36
NG_011806.1:g.38924_38925delinsAG , LRG_553:g.38924_38925delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1245_1246delinsAG MANE Select	ENSP00000356771.3:p.Glu415=
ENST00000367796.3:c.1245_1246delinsAG	ENSP00000356770.3:p.Glu415=
ENST00000367797.7:c.1245_1246delinsAG	ENSP00000356771.3:p.Glu415=
NM_000130.4:c.1245_1246delinsAG , LRG_553t1:c.1245_1246delinsAG	NP_000121.2:p.Glu415=
XM_017000660.2:c.834_835delinsAG	XP_016856149.1:p.Glu278=
NM_000130.5:c.1245_1246delinsAG MANE Select	NP_000121.2:p.Glu415=