Canonical Allele Identifier: CA340883355
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942783G>C , CM000663.2:g.77942783G>C GRCh38
NC_000001.10:g.78408468G>C , CM000663.1:g.78408468G>C GRCh37
NC_000001.9:g.78181056G>C NCBI36
NG_016625.1:g.59269G>C , LRG_442:g.59269G>C
NG_033243.2:g.41311C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1982G>C MANE Select ENSP00000333938.7:p.Gly661Ala
ENST00000330010.12:c.1790G>C ENSP00000327363.8:p.Gly597Ala
ENST00000334785.11:c.1982G>C ENSP00000333938.7:p.Gly661Ala
ENST00000342754.5:c.1681G>C
ENST00000480732.2:n.1556G>C
NM_001172309.1:c.1790G>C NP_001165780.1:p.Gly597Ala
NM_144573.3:c.1982G>C , LRG_442t1:c.1982G>C NP_653174.3:p.Gly661Ala
XM_005271322.2:c.1982G>C XP_005271379.1:p.Gly661Ala
XM_005271323.2:c.1940G>C XP_005271380.1:p.Gly647Ala
XM_005271324.3:c.1790G>C XP_005271381.1:p.Gly597Ala
XM_005271325.2:c.1760G>C XP_005271382.1:p.Gly587Ala
XM_005271326.2:c.1748G>C XP_005271383.1:p.Gly583Ala
XM_005271327.2:c.1565G>C XP_005271384.1:p.Gly522Ala
XM_005271322.4:c.1982G>C XP_005271379.1:p.Gly661Ala
XM_005271323.4:c.1940G>C XP_005271380.1:p.Gly647Ala
XM_005271324.5:c.1790G>C XP_005271381.1:p.Gly597Ala
XM_005271325.4:c.1760G>C XP_005271382.1:p.Gly587Ala
XM_005271326.4:c.1748G>C XP_005271383.1:p.Gly583Ala
XM_005271327.4:c.1565G>C XP_005271384.1:p.Gly522Ala
NM_001172309.2:c.1790G>C NP_001165780.1:p.Gly597Ala
NM_144573.4:c.1982G>C MANE Select NP_653174.3:p.Gly661Ala