Canonical Allele Identifier: CA2646274714
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77935889_77935892dup , CM000663.2:g.77935889_77935892dup GRCh38
NC_000001.10:g.78401574_78401577dup , CM000663.1:g.78401574_78401577dup GRCh37
NC_000001.9:g.78174162_78174165dup NCBI36
NG_016625.1:g.52375_52378dup , LRG_442:g.52375_52378dup

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.1318_1321dup MANE Select ENSP00000333938.7:p.Gly441GlufsTer7
ENST00000330010.12:c.1126_1129dup ENSP00000327363.8:p.Gly377GlufsTer7
ENST00000334785.11:c.1318_1321dup ENSP00000333938.7:p.Gly441GlufsTer7
ENST00000342754.5:c.1017_1020dup
ENST00000440324.5:c.1276_1279dup ENSP00000411902.1:p.Gly427GlufsTer7
ENST00000464998.1:n.778_781dup
ENST00000480732.2:n.892_895dup
NM_001172309.1:c.1126_1129dup NP_001165780.1:p.Gly377GlufsTer7
NM_144573.3:c.1318_1321dup , LRG_442t1:c.1318_1321dup NP_653174.3:p.Gly441GlufsTer7
XM_005271322.2:c.1318_1321dup XP_005271379.1:p.Gly441GlufsTer7
XM_005271323.2:c.1276_1279dup XP_005271380.1:p.Gly427GlufsTer7
XM_005271324.3:c.1126_1129dup XP_005271381.1:p.Gly377GlufsTer7
XM_005271325.2:c.1251+2410_1251+2413dup XP_005271382.1:n.1251+2410_1251+2413dup
XM_005271326.2:c.1084_1087dup XP_005271383.1:p.Gly363GlufsTer7
XM_005271327.2:c.901_904dup XP_005271384.1:p.Gly302GlufsTer7
XM_005271322.4:c.1318_1321dup XP_005271379.1:p.Gly441GlufsTer7
XM_005271323.4:c.1276_1279dup XP_005271380.1:p.Gly427GlufsTer7
XM_005271324.5:c.1126_1129dup XP_005271381.1:p.Gly377GlufsTer7
XM_005271325.4:c.1251+2410_1251+2413dup XP_005271382.1:n.1251+2410_1251+2413dup
XM_005271326.4:c.1084_1087dup XP_005271383.1:p.Gly363GlufsTer7
XM_005271327.4:c.901_904dup XP_005271384.1:p.Gly302GlufsTer7
NM_001172309.2:c.1126_1129dup NP_001165780.1:p.Gly377GlufsTer7
NM_144573.4:c.1318_1321dup MANE Select NP_653174.3:p.Gly441GlufsTer7