Canonical Allele Identifier: CA1177628283
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77935872_77935873delinsTG , CM000663.2:g.77935872_77935873delinsTG GRCh38
NC_000001.10:g.78401557_78401558delinsTG , CM000663.1:g.78401557_78401558delinsTG GRCh37
NC_000001.9:g.78174145_78174146delinsTG NCBI36
NG_016625.1:g.52358_52359delinsTG , LRG_442:g.52358_52359delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1301_1302delinsTG MANE Select ENSP00000333938.7:p.Leu434=
ENST00000330010.12:c.1109_1110delinsTG ENSP00000327363.8:p.Leu370=
ENST00000334785.11:c.1301_1302delinsTG ENSP00000333938.7:p.Leu434=
ENST00000342754.5:c.1000_1001delinsTG
ENST00000440324.5:c.1259_1260delinsTG ENSP00000411902.1:p.Leu420=
ENST00000464998.1:n.761_762delinsTG
ENST00000480732.2:n.875_876delinsTG
NM_001172309.1:c.1109_1110delinsTG NP_001165780.1:p.Leu370=
NM_144573.3:c.1301_1302delinsTG , LRG_442t1:c.1301_1302delinsTG NP_653174.3:p.Leu434=
XM_005271322.2:c.1301_1302delinsTG XP_005271379.1:p.Leu434=
XM_005271323.2:c.1259_1260delinsTG XP_005271380.1:p.Leu420=
XM_005271324.3:c.1109_1110delinsTG XP_005271381.1:p.Leu370=
XM_005271325.2:c.1251+2393_1251+2394delinsTG XP_005271382.1:n.1251+2393_1251+2394delinsTG
XM_005271326.2:c.1067_1068delinsTG XP_005271383.1:p.Leu356=
XM_005271327.2:c.884_885delinsTG XP_005271384.1:p.Leu295=
XM_005271322.4:c.1301_1302delinsTG XP_005271379.1:p.Leu434=
XM_005271323.4:c.1259_1260delinsTG XP_005271380.1:p.Leu420=
XM_005271324.5:c.1109_1110delinsTG XP_005271381.1:p.Leu370=
XM_005271325.4:c.1251+2393_1251+2394delinsTG XP_005271382.1:n.1251+2393_1251+2394delinsTG
XM_005271326.4:c.1067_1068delinsTG XP_005271383.1:p.Leu356=
XM_005271327.4:c.884_885delinsTG XP_005271384.1:p.Leu295=
NM_001172309.2:c.1109_1110delinsTG NP_001165780.1:p.Leu370=
NM_144573.4:c.1301_1302delinsTG MANE Select NP_653174.3:p.Leu434=