Canonical Allele Identifier: CA142174
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 47913
dbSNP Id: rs188416492
gnomAD v2: 1-78392589-T-A
gnomAD v3: 1-77926904-T-A
gnomAD v4: 1-77926904-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77926904T>A , CM000663.2:g.77926904T>A GRCh38
NC_000001.10:g.78392589T>A , CM000663.1:g.78392589T>A GRCh37
NC_000001.9:g.78165177T>A NCBI36
NG_016625.1:g.43390T>A , LRG_442:g.43390T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.864+12T>A MANE Select ENSP00000333938.7:n.864+12T>A
ENST00000330010.12:c.672+12T>A ENSP00000327363.8:n.672+12T>A
ENST00000334785.11:c.864+12T>A ENSP00000333938.7:n.864+12T>A
ENST00000342754.5:c.563+12T>A
ENST00000401035.7:c.672+12T>A ENSP00000383814.3:n.672+12T>A
ENST00000440324.5:c.822+12T>A ENSP00000411902.1:n.822+12T>A
ENST00000464998.1:n.324+12T>A
NM_001172309.1:c.672+12T>A NP_001165780.1:n.672+12T>A
NM_144573.3:c.864+12T>A , LRG_442t1:c.864+12T>A NP_653174.3:n.864+12T>A
XM_005271322.2:c.864+12T>A XP_005271379.1:n.864+12T>A
XM_005271323.2:c.822+12T>A XP_005271380.1:n.822+12T>A
XM_005271324.3:c.672+12T>A XP_005271381.1:n.672+12T>A
XM_005271325.2:c.864+12T>A XP_005271382.1:n.864+12T>A
XM_005271326.2:c.630+12T>A XP_005271383.1:n.630+12T>A
XM_005271327.2:c.448-2412T>A XP_005271384.1:n.448-2412T>A
XM_005271322.4:c.864+12T>A XP_005271379.1:n.864+12T>A
XM_005271323.4:c.822+12T>A XP_005271380.1:n.822+12T>A
XM_005271324.5:c.672+12T>A XP_005271381.1:n.672+12T>A
XM_005271325.4:c.864+12T>A XP_005271382.1:n.864+12T>A
XM_005271326.4:c.630+12T>A XP_005271383.1:n.630+12T>A
XM_005271327.4:c.448-2412T>A XP_005271384.1:n.448-2412T>A
NM_001172309.2:c.672+12T>A NP_001165780.1:n.672+12T>A
NM_144573.4:c.864+12T>A MANE Select NP_653174.3:n.864+12T>A