Canonical Allele Identifier: CA918940
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs762898853
gnomAD v2: 1-78407861-G-A
gnomAD v4: 1-77942176-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942176G>A , CM000663.2:g.77942176G>A GRCh38
NC_000001.10:g.78407861G>A , CM000663.1:g.78407861G>A GRCh37
NC_000001.9:g.78180449G>A NCBI36
NG_016625.1:g.58662G>A , LRG_442:g.58662G>A
NG_033243.2:g.41918C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1627G>A MANE Select ENSP00000333938.7:p.Glu543Lys
ENST00000330010.12:c.1435G>A ENSP00000327363.8:p.Glu479Lys
ENST00000334785.11:c.1627G>A ENSP00000333938.7:p.Glu543Lys
ENST00000342754.5:c.1326G>A
ENST00000470735.1:n.466G>A
ENST00000480732.2:n.1201G>A
NM_001172309.1:c.1435G>A NP_001165780.1:p.Glu479Lys
NM_144573.3:c.1627G>A , LRG_442t1:c.1627G>A NP_653174.3:p.Glu543Lys
XM_005271322.2:c.1627G>A XP_005271379.1:p.Glu543Lys
XM_005271323.2:c.1585G>A XP_005271380.1:p.Glu529Lys
XM_005271324.3:c.1435G>A XP_005271381.1:p.Glu479Lys
XM_005271325.2:c.1405G>A XP_005271382.1:p.Glu469Lys
XM_005271326.2:c.1393G>A XP_005271383.1:p.Glu465Lys
XM_005271327.2:c.1210G>A XP_005271384.1:p.Glu404Lys
XM_005271322.4:c.1627G>A XP_005271379.1:p.Glu543Lys
XM_005271323.4:c.1585G>A XP_005271380.1:p.Glu529Lys
XM_005271324.5:c.1435G>A XP_005271381.1:p.Glu479Lys
XM_005271325.4:c.1405G>A XP_005271382.1:p.Glu469Lys
XM_005271326.4:c.1393G>A XP_005271383.1:p.Glu465Lys
XM_005271327.4:c.1210G>A XP_005271384.1:p.Glu404Lys
NM_001172309.2:c.1435G>A NP_001165780.1:p.Glu479Lys
NM_144573.4:c.1627G>A MANE Select NP_653174.3:p.Glu543Lys