Canonical Allele Identifier: CA1177631182
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942152_77942156delinsCAAAA , CM000663.2:g.77942152_77942156delinsCAAAA GRCh38
NC_000001.10:g.78407837_78407841delinsCAAAA , CM000663.1:g.78407837_78407841delinsCAAAA GRCh37
NC_000001.9:g.78180425_78180429delinsCAAAA NCBI36
NG_016625.1:g.58638_58642delinsCAAAA , LRG_442:g.58638_58642delinsCAAAA
NG_033243.2:g.41938_41942delinsTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1603_1607delinsCAAAA MANE Select ENSP00000333938.7:p.Gln535=
ENST00000330010.12:c.1411_1415delinsCAAAA ENSP00000327363.8:p.Gln471=
ENST00000334785.11:c.1603_1607delinsCAAAA ENSP00000333938.7:p.Gln535=
ENST00000342754.5:c.1302_1306delinsCAAAA
ENST00000470735.1:n.442_446delinsCAAAA
ENST00000480732.2:n.1177_1181delinsCAAAA
NM_001172309.1:c.1411_1415delinsCAAAA NP_001165780.1:p.Gln471=
NM_144573.3:c.1603_1607delinsCAAAA , LRG_442t1:c.1603_1607delinsCAAAA NP_653174.3:p.Gln535=
XM_005271322.2:c.1603_1607delinsCAAAA XP_005271379.1:p.Gln535=
XM_005271323.2:c.1561_1565delinsCAAAA XP_005271380.1:p.Gln521=
XM_005271324.3:c.1411_1415delinsCAAAA XP_005271381.1:p.Gln471=
XM_005271325.2:c.1381_1385delinsCAAAA XP_005271382.1:p.Gln461=
XM_005271326.2:c.1369_1373delinsCAAAA XP_005271383.1:p.Gln457=
XM_005271327.2:c.1186_1190delinsCAAAA XP_005271384.1:p.Gln396=
XM_005271322.4:c.1603_1607delinsCAAAA XP_005271379.1:p.Gln535=
XM_005271323.4:c.1561_1565delinsCAAAA XP_005271380.1:p.Gln521=
XM_005271324.5:c.1411_1415delinsCAAAA XP_005271381.1:p.Gln471=
XM_005271325.4:c.1381_1385delinsCAAAA XP_005271382.1:p.Gln461=
XM_005271326.4:c.1369_1373delinsCAAAA XP_005271383.1:p.Gln457=
XM_005271327.4:c.1186_1190delinsCAAAA XP_005271384.1:p.Gln396=
NM_001172309.2:c.1411_1415delinsCAAAA NP_001165780.1:p.Gln471=
NM_144573.4:c.1603_1607delinsCAAAA MANE Select NP_653174.3:p.Gln535=