Canonical Allele Identifier: CA340881350
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942156A>C , CM000663.2:g.77942156A>C GRCh38
NC_000001.10:g.78407841A>C , CM000663.1:g.78407841A>C GRCh37
NC_000001.9:g.78180429A>C NCBI36
NG_016625.1:g.58642A>C , LRG_442:g.58642A>C
NG_033243.2:g.41938T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1607A>C MANE Select ENSP00000333938.7:p.Lys536Thr
ENST00000330010.12:c.1415A>C ENSP00000327363.8:p.Lys472Thr
ENST00000334785.11:c.1607A>C ENSP00000333938.7:p.Lys536Thr
ENST00000342754.5:c.1306A>C
ENST00000470735.1:n.446A>C
ENST00000480732.2:n.1181A>C
NM_001172309.1:c.1415A>C NP_001165780.1:p.Lys472Thr
NM_144573.3:c.1607A>C , LRG_442t1:c.1607A>C NP_653174.3:p.Lys536Thr
XM_005271322.2:c.1607A>C XP_005271379.1:p.Lys536Thr
XM_005271323.2:c.1565A>C XP_005271380.1:p.Lys522Thr
XM_005271324.3:c.1415A>C XP_005271381.1:p.Lys472Thr
XM_005271325.2:c.1385A>C XP_005271382.1:p.Lys462Thr
XM_005271326.2:c.1373A>C XP_005271383.1:p.Lys458Thr
XM_005271327.2:c.1190A>C XP_005271384.1:p.Lys397Thr
XM_005271322.4:c.1607A>C XP_005271379.1:p.Lys536Thr
XM_005271323.4:c.1565A>C XP_005271380.1:p.Lys522Thr
XM_005271324.5:c.1415A>C XP_005271381.1:p.Lys472Thr
XM_005271325.4:c.1385A>C XP_005271382.1:p.Lys462Thr
XM_005271326.4:c.1373A>C XP_005271383.1:p.Lys458Thr
XM_005271327.4:c.1190A>C XP_005271384.1:p.Lys397Thr
NM_001172309.2:c.1415A>C NP_001165780.1:p.Lys472Thr
NM_144573.4:c.1607A>C MANE Select NP_653174.3:p.Lys536Thr