Canonical Allele Identifier: CA1177628433

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936203_77936205delinsCTT , CM000663.2:g.77936203_77936205delinsCTT	GRCh38
NC_000001.10:g.78401888_78401890delinsCTT , CM000663.1:g.78401888_78401890delinsCTT	GRCh37
NC_000001.9:g.78174476_78174478delinsCTT	NCBI36
NG_016625.1:g.52689_52691delinsCTT , LRG_442:g.52689_52691delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+159_1473+161delinsCTT MANE Select	ENSP00000333938.7:n.1473+159_1473+161delinsCTT
ENST00000330010.12:c.1281+159_1281+161delinsCTT	ENSP00000327363.8:n.1281+159_1281+161delinsCTT
ENST00000334785.11:c.1473+159_1473+161delinsCTT	ENSP00000333938.7:n.1473+159_1473+161delinsCTT
ENST00000342754.5:c.1172+159_1172+161delinsCTT
ENST00000480732.2:n.1047+159_1047+161delinsCTT
NM_001172309.1:c.1281+159_1281+161delinsCTT	NP_001165780.1:n.1281+159_1281+161delinsCTT
NM_144573.3:c.1473+159_1473+161delinsCTT , LRG_442t1:c.1473+159_1473+161delinsCTT	NP_653174.3:n.1473+159_1473+161delinsCTT
XM_005271322.2:c.1473+159_1473+161delinsCTT	XP_005271379.1:n.1473+159_1473+161delinsCTT
XM_005271323.2:c.1431+159_1431+161delinsCTT	XP_005271380.1:n.1431+159_1431+161delinsCTT
XM_005271324.3:c.1281+159_1281+161delinsCTT	XP_005271381.1:n.1281+159_1281+161delinsCTT
XM_005271325.2:c.1251+2724_1251+2726delinsCTT	XP_005271382.1:n.1251+2724_1251+2726delinsCTT
XM_005271326.2:c.1239+159_1239+161delinsCTT	XP_005271383.1:n.1239+159_1239+161delinsCTT
XM_005271327.2:c.1056+159_1056+161delinsCTT	XP_005271384.1:n.1056+159_1056+161delinsCTT
XM_005271322.4:c.1473+159_1473+161delinsCTT	XP_005271379.1:n.1473+159_1473+161delinsCTT
XM_005271323.4:c.1431+159_1431+161delinsCTT	XP_005271380.1:n.1431+159_1431+161delinsCTT
XM_005271324.5:c.1281+159_1281+161delinsCTT	XP_005271381.1:n.1281+159_1281+161delinsCTT
XM_005271325.4:c.1251+2724_1251+2726delinsCTT	XP_005271382.1:n.1251+2724_1251+2726delinsCTT
XM_005271326.4:c.1239+159_1239+161delinsCTT	XP_005271383.1:n.1239+159_1239+161delinsCTT
XM_005271327.4:c.1056+159_1056+161delinsCTT	XP_005271384.1:n.1056+159_1056+161delinsCTT
NM_001172309.2:c.1281+159_1281+161delinsCTT	NP_001165780.1:n.1281+159_1281+161delinsCTT
NM_144573.4:c.1473+159_1473+161delinsCTT MANE Select	NP_653174.3:n.1473+159_1473+161delinsCTT