Canonical Allele Identifier: CA24686884
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs533124149
gnomAD v2: 1-78401993-C-T
gnomAD v3: 1-77936308-C-T
gnomAD v4: 1-77936308-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77936308C>T , CM000663.2:g.77936308C>T GRCh38
NC_000001.10:g.78401993C>T , CM000663.1:g.78401993C>T GRCh37
NC_000001.9:g.78174581C>T NCBI36
NG_016625.1:g.52794C>T , LRG_442:g.52794C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1473+264C>T MANE Select ENSP00000333938.7:n.1473+264C>T
ENST00000330010.12:c.1281+264C>T ENSP00000327363.8:n.1281+264C>T
ENST00000334785.11:c.1473+264C>T ENSP00000333938.7:n.1473+264C>T
ENST00000342754.5:c.1172+264C>T
ENST00000480732.2:n.1047+264C>T
NM_001172309.1:c.1281+264C>T NP_001165780.1:n.1281+264C>T
NM_144573.3:c.1473+264C>T , LRG_442t1:c.1473+264C>T NP_653174.3:n.1473+264C>T
XM_005271322.2:c.1473+264C>T XP_005271379.1:n.1473+264C>T
XM_005271323.2:c.1431+264C>T XP_005271380.1:n.1431+264C>T
XM_005271324.3:c.1281+264C>T XP_005271381.1:n.1281+264C>T
XM_005271325.2:c.1251+2829C>T XP_005271382.1:n.1251+2829C>T
XM_005271326.2:c.1239+264C>T XP_005271383.1:n.1239+264C>T
XM_005271327.2:c.1056+264C>T XP_005271384.1:n.1056+264C>T
XM_005271322.4:c.1473+264C>T XP_005271379.1:n.1473+264C>T
XM_005271323.4:c.1431+264C>T XP_005271380.1:n.1431+264C>T
XM_005271324.5:c.1281+264C>T XP_005271381.1:n.1281+264C>T
XM_005271325.4:c.1251+2829C>T XP_005271382.1:n.1251+2829C>T
XM_005271326.4:c.1239+264C>T XP_005271383.1:n.1239+264C>T
XM_005271327.4:c.1056+264C>T XP_005271384.1:n.1056+264C>T
NM_001172309.2:c.1281+264C>T NP_001165780.1:n.1281+264C>T
NM_144573.4:c.1473+264C>T MANE Select NP_653174.3:n.1473+264C>T