Canonical Allele Identifier: CA1177628240
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77935790_77935791delinsCA , CM000663.2:g.77935790_77935791delinsCA GRCh38
NC_000001.10:g.78401475_78401476delinsCA , CM000663.1:g.78401475_78401476delinsCA GRCh37
NC_000001.9:g.78174063_78174064delinsCA NCBI36
NG_016625.1:g.52276_52277delinsCA , LRG_442:g.52276_52277delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1252-33_1252-32delinsCA MANE Select ENSP00000333938.7:n.1252-33_1252-32delinsCA
ENST00000330010.12:c.1060-33_1060-32delinsCA ENSP00000327363.8:n.1060-33_1060-32delinsCA
ENST00000334785.11:c.1252-33_1252-32delinsCA ENSP00000333938.7:n.1252-33_1252-32delinsCA
ENST00000342754.5:c.951-33_951-32delinsCA
ENST00000440324.5:c.1210-33_1210-32delinsCA ENSP00000411902.1:n.1210-33_1210-32delinsCA
ENST00000464998.1:n.712-33_712-32delinsCA
ENST00000480732.2:n.826-33_826-32delinsCA
NM_001172309.1:c.1060-33_1060-32delinsCA NP_001165780.1:n.1060-33_1060-32delinsCA
NM_144573.3:c.1252-33_1252-32delinsCA , LRG_442t1:c.1252-33_1252-32delinsCA NP_653174.3:n.1252-33_1252-32delinsCA
XM_005271322.2:c.1252-33_1252-32delinsCA XP_005271379.1:n.1252-33_1252-32delinsCA
XM_005271323.2:c.1210-33_1210-32delinsCA XP_005271380.1:n.1210-33_1210-32delinsCA
XM_005271324.3:c.1060-33_1060-32delinsCA XP_005271381.1:n.1060-33_1060-32delinsCA
XM_005271325.2:c.1251+2311_1251+2312delinsCA XP_005271382.1:n.1251+2311_1251+2312delinsCA
XM_005271326.2:c.1018-33_1018-32delinsCA XP_005271383.1:n.1018-33_1018-32delinsCA
XM_005271327.2:c.835-33_835-32delinsCA XP_005271384.1:n.835-33_835-32delinsCA
XM_005271322.4:c.1252-33_1252-32delinsCA XP_005271379.1:n.1252-33_1252-32delinsCA
XM_005271323.4:c.1210-33_1210-32delinsCA XP_005271380.1:n.1210-33_1210-32delinsCA
XM_005271324.5:c.1060-33_1060-32delinsCA XP_005271381.1:n.1060-33_1060-32delinsCA
XM_005271325.4:c.1251+2311_1251+2312delinsCA XP_005271382.1:n.1251+2311_1251+2312delinsCA
XM_005271326.4:c.1018-33_1018-32delinsCA XP_005271383.1:n.1018-33_1018-32delinsCA
XM_005271327.4:c.835-33_835-32delinsCA XP_005271384.1:n.835-33_835-32delinsCA
NM_001172309.2:c.1060-33_1060-32delinsCA NP_001165780.1:n.1060-33_1060-32delinsCA
NM_144573.4:c.1252-33_1252-32delinsCA MANE Select NP_653174.3:n.1252-33_1252-32delinsCA