Canonical Allele Identifier: CA1206148566

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572198_169572199delinsGA , CM000663.2:g.169572198_169572199delinsGA	GRCh38
NC_000001.10:g.169541436_169541437delinsGA , CM000663.1:g.169541436_169541437delinsGA	GRCh37
NC_000001.9:g.167808060_167808061delinsGA	NCBI36
NG_011806.1:g.19333_19334delinsTC , LRG_553:g.19333_19334delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.373+22_373+23delinsTC MANE Select	ENSP00000356771.3:n.373+22_373+23delinsTC
ENST00000367796.3:c.373+22_373+23delinsTC	ENSP00000356770.3:n.373+22_373+23delinsTC
ENST00000367797.7:c.373+22_373+23delinsTC	ENSP00000356771.3:n.373+22_373+23delinsTC
NM_000130.4:c.373+22_373+23delinsTC , LRG_553t1:c.373+22_373+23delinsTC	NP_000121.2:n.373+22_373+23delinsTC
XM_017000660.2:c.-39+22_-39+23delinsTC	XP_016856149.1:n.-39+22_-39+23delinsTC
NM_000130.5:c.373+22_373+23delinsTC MANE Select	NP_000121.2:n.373+22_373+23delinsTC