Canonical Allele Identifier: CA1206144038

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549631_169549632delinsAG , CM000663.2:g.169549631_169549632delinsAG	GRCh38
NC_000001.10:g.169518869_169518870delinsAG , CM000663.1:g.169518869_169518870delinsAG	GRCh37
NC_000001.9:g.167785493_167785494delinsAG	NCBI36
NG_011806.1:g.41900_41901delinsCT , LRG_553:g.41900_41901delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.1611+169_1611+170delinsCT MANE Select	ENSP00000356771.3:n.1611+169_1611+170delinsCT
ENST00000367796.3:c.1611+169_1611+170delinsCT	ENSP00000356770.3:n.1611+169_1611+170delinsCT
ENST00000367797.7:c.1611+169_1611+170delinsCT	ENSP00000356771.3:n.1611+169_1611+170delinsCT
NM_000130.4:c.1611+169_1611+170delinsCT , LRG_553t1:c.1611+169_1611+170delinsCT	NP_000121.2:n.1611+169_1611+170delinsCT
XM_017000660.2:c.1200+169_1200+170delinsCT	XP_016856149.1:n.1200+169_1200+170delinsCT
NM_000130.5:c.1611+169_1611+170delinsCT MANE Select	NP_000121.2:n.1611+169_1611+170delinsCT