Canonical Allele Identifier: CA340886591
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77918204A>C , CM000663.2:g.77918204A>C GRCh38
NC_000001.10:g.78383889A>C , CM000663.1:g.78383889A>C GRCh37
NC_000001.9:g.78156477A>C NCBI36
NG_016625.1:g.34690A>C , LRG_442:g.34690A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.378A>C MANE Select ENSP00000333938.7:p.Lys126Asn
ENST00000330010.12:c.186A>C ENSP00000327363.8:p.Lys62Asn
ENST00000334785.11:c.378A>C ENSP00000333938.7:p.Lys126Asn
ENST00000342754.5:c.77A>C
ENST00000401035.7:c.186A>C ENSP00000383814.3:p.Lys62Asn
ENST00000440324.5:c.378A>C ENSP00000411902.1:p.Lys126Asn
NM_001172309.1:c.186A>C NP_001165780.1:p.Lys62Asn
NM_144573.3:c.378A>C , LRG_442t1:c.378A>C NP_653174.3:p.Lys126Asn
XM_005271322.2:c.378A>C XP_005271379.1:p.Lys126Asn
XM_005271323.2:c.378A>C XP_005271380.1:p.Lys126Asn
XM_005271324.3:c.186A>C XP_005271381.1:p.Lys62Asn
XM_005271325.2:c.378A>C XP_005271382.1:p.Lys126Asn
XM_005271326.2:c.186A>C XP_005271383.1:p.Lys62Asn
XM_005271327.2:c.378A>C XP_005271384.1:p.Lys126Asn
XM_005271322.4:c.378A>C XP_005271379.1:p.Lys126Asn
XM_005271323.4:c.378A>C XP_005271380.1:p.Lys126Asn
XM_005271324.5:c.186A>C XP_005271381.1:p.Lys62Asn
XM_005271325.4:c.378A>C XP_005271382.1:p.Lys126Asn
XM_005271326.4:c.186A>C XP_005271383.1:p.Lys62Asn
XM_005271327.4:c.378A>C XP_005271384.1:p.Lys126Asn
NM_001172309.2:c.186A>C NP_001165780.1:p.Lys62Asn
NM_144573.4:c.378A>C MANE Select NP_653174.3:p.Lys126Asn