Canonical Allele Identifier: CA918923
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs763106647
gnomAD v2: 1-78407787-A-T
gnomAD v4: 1-77942102-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942102A>T , CM000663.2:g.77942102A>T GRCh38
NC_000001.10:g.78407787A>T , CM000663.1:g.78407787A>T GRCh37
NC_000001.9:g.78180375A>T NCBI36
NG_016625.1:g.58588A>T , LRG_442:g.58588A>T
NG_033243.2:g.41992T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1553A>T MANE Select ENSP00000333938.7:p.Glu518Val
ENST00000330010.12:c.1361A>T ENSP00000327363.8:p.Glu454Val
ENST00000334785.11:c.1553A>T ENSP00000333938.7:p.Glu518Val
ENST00000342754.5:c.1252A>T
ENST00000470735.1:n.392A>T
ENST00000480732.2:n.1127A>T
NM_001172309.1:c.1361A>T NP_001165780.1:p.Glu454Val
NM_144573.3:c.1553A>T , LRG_442t1:c.1553A>T NP_653174.3:p.Glu518Val
XM_005271322.2:c.1553A>T XP_005271379.1:p.Glu518Val
XM_005271323.2:c.1511A>T XP_005271380.1:p.Glu504Val
XM_005271324.3:c.1361A>T XP_005271381.1:p.Glu454Val
XM_005271325.2:c.1331A>T XP_005271382.1:p.Glu444Val
XM_005271326.2:c.1319A>T XP_005271383.1:p.Glu440Val
XM_005271327.2:c.1136A>T XP_005271384.1:p.Glu379Val
XM_005271322.4:c.1553A>T XP_005271379.1:p.Glu518Val
XM_005271323.4:c.1511A>T XP_005271380.1:p.Glu504Val
XM_005271324.5:c.1361A>T XP_005271381.1:p.Glu454Val
XM_005271325.4:c.1331A>T XP_005271382.1:p.Glu444Val
XM_005271326.4:c.1319A>T XP_005271383.1:p.Glu440Val
XM_005271327.4:c.1136A>T XP_005271384.1:p.Glu379Val
NM_001172309.2:c.1361A>T NP_001165780.1:p.Glu454Val
NM_144573.4:c.1553A>T MANE Select NP_653174.3:p.Glu518Val