Canonical Allele Identifier: CA184102
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 179277
dbSNP Id: rs727504758
gnomAD v2: 1-78407762-A-G
gnomAD v4: 1-77942077-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942077A>G , CM000663.2:g.77942077A>G GRCh38
NC_000001.10:g.78407762A>G , CM000663.1:g.78407762A>G GRCh37
NC_000001.9:g.78180350A>G NCBI36
NG_016625.1:g.58563A>G , LRG_442:g.58563A>G
NG_033243.2:g.42017T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.1528A>G MANE Select ENSP00000333938.7:p.Lys510Glu
ENST00000330010.12:c.1336A>G ENSP00000327363.8:p.Lys446Glu
ENST00000334785.11:c.1528A>G ENSP00000333938.7:p.Lys510Glu
ENST00000342754.5:c.1227A>G
ENST00000470735.1:n.367A>G
ENST00000480732.2:n.1102A>G
NM_001172309.1:c.1336A>G NP_001165780.1:p.Lys446Glu
NM_144573.3:c.1528A>G , LRG_442t1:c.1528A>G NP_653174.3:p.Lys510Glu
XM_005271322.2:c.1528A>G XP_005271379.1:p.Lys510Glu
XM_005271323.2:c.1486A>G XP_005271380.1:p.Lys496Glu
XM_005271324.3:c.1336A>G XP_005271381.1:p.Lys446Glu
XM_005271325.2:c.1306A>G XP_005271382.1:p.Lys436Glu
XM_005271326.2:c.1294A>G XP_005271383.1:p.Lys432Glu
XM_005271327.2:c.1111A>G XP_005271384.1:p.Lys371Glu
XM_005271322.4:c.1528A>G XP_005271379.1:p.Lys510Glu
XM_005271323.4:c.1486A>G XP_005271380.1:p.Lys496Glu
XM_005271324.5:c.1336A>G XP_005271381.1:p.Lys446Glu
XM_005271325.4:c.1306A>G XP_005271382.1:p.Lys436Glu
XM_005271326.4:c.1294A>G XP_005271383.1:p.Lys432Glu
XM_005271327.4:c.1111A>G XP_005271384.1:p.Lys371Glu
NM_001172309.2:c.1336A>G NP_001165780.1:p.Lys446Glu
NM_144573.4:c.1528A>G MANE Select NP_653174.3:p.Lys510Glu