Canonical Allele Identifier: CA918878
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs762192995
gnomAD v2: 1-78401701-A-G
gnomAD v4: 1-77936016-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77936016A>G , CM000663.2:g.77936016A>G GRCh38
NC_000001.10:g.78401701A>G , CM000663.1:g.78401701A>G GRCh37
NC_000001.9:g.78174289A>G NCBI36
NG_016625.1:g.52502A>G , LRG_442:g.52502A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1445A>G MANE Select ENSP00000333938.7:p.Lys482Arg
ENST00000330010.12:c.1253A>G ENSP00000327363.8:p.Lys418Arg
ENST00000334785.11:c.1445A>G ENSP00000333938.7:p.Lys482Arg
ENST00000342754.5:c.1144A>G
ENST00000480732.2:n.1019A>G
NM_001172309.1:c.1253A>G NP_001165780.1:p.Lys418Arg
NM_144573.3:c.1445A>G , LRG_442t1:c.1445A>G NP_653174.3:p.Lys482Arg
XM_005271322.2:c.1445A>G XP_005271379.1:p.Lys482Arg
XM_005271323.2:c.1403A>G XP_005271380.1:p.Lys468Arg
XM_005271324.3:c.1253A>G XP_005271381.1:p.Lys418Arg
XM_005271325.2:c.1251+2537A>G XP_005271382.1:n.1251+2537A>G
XM_005271326.2:c.1211A>G XP_005271383.1:p.Lys404Arg
XM_005271327.2:c.1028A>G XP_005271384.1:p.Lys343Arg
XM_005271322.4:c.1445A>G XP_005271379.1:p.Lys482Arg
XM_005271323.4:c.1403A>G XP_005271380.1:p.Lys468Arg
XM_005271324.5:c.1253A>G XP_005271381.1:p.Lys418Arg
XM_005271325.4:c.1251+2537A>G XP_005271382.1:n.1251+2537A>G
XM_005271326.4:c.1211A>G XP_005271383.1:p.Lys404Arg
XM_005271327.4:c.1028A>G XP_005271384.1:p.Lys343Arg
NM_001172309.2:c.1253A>G NP_001165780.1:p.Lys418Arg
NM_144573.4:c.1445A>G MANE Select NP_653174.3:p.Lys482Arg