Canonical Allele Identifier: CA177495
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 164797
dbSNP Id: rs727503346
gnomAD v4: 1-77942688-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942688A>G , CM000663.2:g.77942688A>G GRCh38
NC_000001.10:g.78408373A>G , CM000663.1:g.78408373A>G GRCh37
NC_000001.9:g.78180961A>G NCBI36
NG_016625.1:g.59174A>G , LRG_442:g.59174A>G
NG_033243.2:g.41406T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.1887A>G MANE Select ENSP00000333938.7:p.Gln629=
ENST00000330010.12:c.1695A>G ENSP00000327363.8:p.Gln565=
ENST00000334785.11:c.1887A>G ENSP00000333938.7:p.Gln629=
ENST00000342754.5:c.1586A>G
ENST00000470735.1:n.726A>G
ENST00000480732.2:n.1461A>G
NM_001172309.1:c.1695A>G NP_001165780.1:p.Gln565=
NM_144573.3:c.1887A>G , LRG_442t1:c.1887A>G NP_653174.3:p.Gln629=
XM_005271322.2:c.1887A>G XP_005271379.1:p.Gln629=
XM_005271323.2:c.1845A>G XP_005271380.1:p.Gln615=
XM_005271324.3:c.1695A>G XP_005271381.1:p.Gln565=
XM_005271325.2:c.1665A>G XP_005271382.1:p.Gln555=
XM_005271326.2:c.1653A>G XP_005271383.1:p.Gln551=
XM_005271327.2:c.1470A>G XP_005271384.1:p.Gln490=
XM_005271322.4:c.1887A>G XP_005271379.1:p.Gln629=
XM_005271323.4:c.1845A>G XP_005271380.1:p.Gln615=
XM_005271324.5:c.1695A>G XP_005271381.1:p.Gln565=
XM_005271325.4:c.1665A>G XP_005271382.1:p.Gln555=
XM_005271326.4:c.1653A>G XP_005271383.1:p.Gln551=
XM_005271327.4:c.1470A>G XP_005271384.1:p.Gln490=
NM_001172309.2:c.1695A>G NP_001165780.1:p.Gln565=
NM_144573.4:c.1887A>G MANE Select NP_653174.3:p.Gln629=