Canonical Allele Identifier: CA2586966785

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935970_77935972del , CM000663.2:g.77935970_77935972del	GRCh38
NC_000001.10:g.78401655_78401657del , CM000663.1:g.78401655_78401657del	GRCh37
NC_000001.9:g.78174243_78174245del	NCBI36
NG_016625.1:g.52456_52458del , LRG_442:g.52456_52458del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1399_1401del MANE Select	ENSP00000333938.7:p.Ile467del
ENST00000330010.12:c.1207_1209del	ENSP00000327363.8:p.Ile403del
ENST00000334785.11:c.1399_1401del	ENSP00000333938.7:p.Ile467del
ENST00000342754.5:c.1098_1100del
ENST00000480732.2:n.973_975del
NM_001172309.1:c.1207_1209del	NP_001165780.1:p.Ile403del
NM_144573.3:c.1399_1401del , LRG_442t1:c.1399_1401del	NP_653174.3:p.Ile467del
XM_005271322.2:c.1399_1401del	XP_005271379.1:p.Ile467del
XM_005271323.2:c.1357_1359del	XP_005271380.1:p.Ile453del
XM_005271324.3:c.1207_1209del	XP_005271381.1:p.Ile403del
XM_005271325.2:c.1251+2491_1251+2493del	XP_005271382.1:n.1251+2491_1251+2493del
XM_005271326.2:c.1165_1167del	XP_005271383.1:p.Ile389del
XM_005271327.2:c.982_984del	XP_005271384.1:p.Ile328del
XM_005271322.4:c.1399_1401del	XP_005271379.1:p.Ile467del
XM_005271323.4:c.1357_1359del	XP_005271380.1:p.Ile453del
XM_005271324.5:c.1207_1209del	XP_005271381.1:p.Ile403del
XM_005271325.4:c.1251+2491_1251+2493del	XP_005271382.1:n.1251+2491_1251+2493del
XM_005271326.4:c.1165_1167del	XP_005271383.1:p.Ile389del
XM_005271327.4:c.982_984del	XP_005271384.1:p.Ile328del
NM_001172309.2:c.1207_1209del	NP_001165780.1:p.Ile403del
NM_144573.4:c.1399_1401del MANE Select	NP_653174.3:p.Ile467del