Canonical Allele Identifier: CA1177626266
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942887_77942889delinsTTC , CM000663.2:g.77942887_77942889delinsTTC GRCh38
NC_000001.10:g.78408572_78408574delinsTTC , CM000663.1:g.78408572_78408574delinsTTC GRCh37
NC_000001.9:g.78181160_78181162delinsTTC NCBI36
NG_016625.1:g.59373_59375delinsTTC , LRG_442:g.59373_59375delinsTTC
NG_033243.2:g.41205_41207delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.*58_*60delinsTTC MANE Select ENSP00000333938.7:n.*58_*60delinsTTC
ENST00000330010.12:c.*58_*60delinsTTC ENSP00000327363.8:n.*58_*60delinsTTC
ENST00000334785.11:c.*58_*60delinsTTC ENSP00000333938.7:n.*58_*60delinsTTC
ENST00000342754.5:c.1717-13_1717-11delinsTTC
ENST00000480732.2:n.1660_1662delinsTTC
NM_001172309.1:c.*58_*60delinsTTC NP_001165780.1:n.*58_*60delinsTTC
NM_144573.3:c.*58_*60delinsTTC , LRG_442t1:c.*58_*60delinsTTC NP_653174.3:n.*58_*60delinsTTC
XM_005271322.2:c.2018-13_2018-11delinsTTC XP_005271379.1:n.2018-13_2018-11delinsTTC
XM_005271323.2:c.1976-13_1976-11delinsTTC XP_005271380.1:n.1976-13_1976-11delinsTTC
XM_005271324.3:c.1826-13_1826-11delinsTTC XP_005271381.1:n.1826-13_1826-11delinsTTC
XM_005271325.2:c.1796-13_1796-11delinsTTC XP_005271382.1:n.1796-13_1796-11delinsTTC
XM_005271326.2:c.1784-13_1784-11delinsTTC XP_005271383.1:n.1784-13_1784-11delinsTTC
XM_005271327.2:c.1601-13_1601-11delinsTTC XP_005271384.1:n.1601-13_1601-11delinsTTC
XM_005271322.4:c.2018-13_2018-11delinsTTC XP_005271379.1:n.2018-13_2018-11delinsTTC
XM_005271323.4:c.1976-13_1976-11delinsTTC XP_005271380.1:n.1976-13_1976-11delinsTTC
XM_005271324.5:c.1826-13_1826-11delinsTTC XP_005271381.1:n.1826-13_1826-11delinsTTC
XM_005271325.4:c.1796-13_1796-11delinsTTC XP_005271382.1:n.1796-13_1796-11delinsTTC
XM_005271326.4:c.1784-13_1784-11delinsTTC XP_005271383.1:n.1784-13_1784-11delinsTTC
XM_005271327.4:c.1601-13_1601-11delinsTTC XP_005271384.1:n.1601-13_1601-11delinsTTC
NM_001172309.2:c.*58_*60delinsTTC NP_001165780.1:n.*58_*60delinsTTC
NM_144573.4:c.*58_*60delinsTTC MANE Select NP_653174.3:n.*58_*60delinsTTC