Canonical Allele Identifier: CA2646274716

Gene: NEXN

Linked Data

• gnomAD v4: 1-77935990-AAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935993_77935995del , CM000663.2:g.77935993_77935995del	GRCh38
NC_000001.10:g.78401678_78401680del , CM000663.1:g.78401678_78401680del	GRCh37
NC_000001.9:g.78174266_78174268del	NCBI36
NG_016625.1:g.52479_52481del , LRG_442:g.52479_52481del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1422_1424del MANE Select	ENSP00000333938.7:p.Arg475del
ENST00000330010.12:c.1230_1232del	ENSP00000327363.8:p.Arg411del
ENST00000334785.11:c.1422_1424del	ENSP00000333938.7:p.Arg475del
ENST00000342754.5:c.1121_1123del
ENST00000480732.2:n.996_998del
NM_001172309.1:c.1230_1232del	NP_001165780.1:p.Arg411del
NM_144573.3:c.1422_1424del , LRG_442t1:c.1422_1424del	NP_653174.3:p.Arg475del
XM_005271322.2:c.1422_1424del	XP_005271379.1:p.Arg475del
XM_005271323.2:c.1380_1382del	XP_005271380.1:p.Arg461del
XM_005271324.3:c.1230_1232del	XP_005271381.1:p.Arg411del
XM_005271325.2:c.1251+2514_1251+2516del	XP_005271382.1:n.1251+2514_1251+2516del
XM_005271326.2:c.1188_1190del	XP_005271383.1:p.Arg397del
XM_005271327.2:c.1005_1007del	XP_005271384.1:p.Arg336del
XM_005271322.4:c.1422_1424del	XP_005271379.1:p.Arg475del
XM_005271323.4:c.1380_1382del	XP_005271380.1:p.Arg461del
XM_005271324.5:c.1230_1232del	XP_005271381.1:p.Arg411del
XM_005271325.4:c.1251+2514_1251+2516del	XP_005271382.1:n.1251+2514_1251+2516del
XM_005271326.4:c.1188_1190del	XP_005271383.1:p.Arg397del
XM_005271327.4:c.1005_1007del	XP_005271384.1:p.Arg336del
NM_001172309.2:c.1230_1232del	NP_001165780.1:p.Arg411del
NM_144573.4:c.1422_1424del MANE Select	NP_653174.3:p.Arg475del