Canonical Allele Identifier: CA24678118
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs1033247134

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77926359T>C , CM000663.2:g.77926359T>C GRCh38
NC_000001.10:g.78392044T>C , CM000663.1:g.78392044T>C GRCh37
NC_000001.9:g.78164632T>C NCBI36
NG_016625.1:g.42845T>C , LRG_442:g.42845T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.490-55T>C MANE Select ENSP00000333938.7:n.490-55T>C
ENST00000330010.12:c.298-55T>C ENSP00000327363.8:n.298-55T>C
ENST00000334785.11:c.490-55T>C ENSP00000333938.7:n.490-55T>C
ENST00000342754.5:c.189-55T>C
ENST00000401035.7:c.298-55T>C ENSP00000383814.3:n.298-55T>C
ENST00000440324.5:c.448-55T>C ENSP00000411902.1:n.448-55T>C
NM_001172309.1:c.298-55T>C NP_001165780.1:n.298-55T>C
NM_144573.3:c.490-55T>C , LRG_442t1:c.490-55T>C NP_653174.3:n.490-55T>C
XM_005271322.2:c.490-55T>C XP_005271379.1:n.490-55T>C
XM_005271323.2:c.448-55T>C XP_005271380.1:n.448-55T>C
XM_005271324.3:c.298-55T>C XP_005271381.1:n.298-55T>C
XM_005271325.2:c.490-55T>C XP_005271382.1:n.490-55T>C
XM_005271326.2:c.256-55T>C XP_005271383.1:n.256-55T>C
XM_005271327.2:c.448-2957T>C XP_005271384.1:n.448-2957T>C
XM_005271322.4:c.490-55T>C XP_005271379.1:n.490-55T>C
XM_005271323.4:c.448-55T>C XP_005271380.1:n.448-55T>C
XM_005271324.5:c.298-55T>C XP_005271381.1:n.298-55T>C
XM_005271325.4:c.490-55T>C XP_005271382.1:n.490-55T>C
XM_005271326.4:c.256-55T>C XP_005271383.1:n.256-55T>C
XM_005271327.4:c.448-2957T>C XP_005271384.1:n.448-2957T>C
NM_001172309.2:c.298-55T>C NP_001165780.1:n.298-55T>C
NM_144573.4:c.490-55T>C MANE Select NP_653174.3:n.490-55T>C