Canonical Allele Identifier: CA918827
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 229053
dbSNP Id: rs768693715
gnomAD v2: 1-78399147-A-G
gnomAD v4: 1-77933462-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77933462A>G , CM000663.2:g.77933462A>G GRCh38
NC_000001.10:g.78399147A>G , CM000663.1:g.78399147A>G GRCh37
NC_000001.9:g.78171735A>G NCBI36
NG_016625.1:g.49948A>G , LRG_442:g.49948A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.1234A>G MANE Select ENSP00000333938.7:p.Arg412Gly
ENST00000330010.12:c.1042A>G ENSP00000327363.8:p.Arg348Gly
ENST00000334785.11:c.1234A>G ENSP00000333938.7:p.Arg412Gly
ENST00000342754.5:c.933A>G
ENST00000440324.5:c.1192A>G ENSP00000411902.1:p.Arg398Gly
ENST00000464998.1:n.694A>G
ENST00000480732.2:n.808A>G
NM_001172309.1:c.1042A>G NP_001165780.1:p.Arg348Gly
NM_144573.3:c.1234A>G , LRG_442t1:c.1234A>G NP_653174.3:p.Arg412Gly
XM_005271322.2:c.1234A>G XP_005271379.1:p.Arg412Gly
XM_005271323.2:c.1192A>G XP_005271380.1:p.Arg398Gly
XM_005271324.3:c.1042A>G XP_005271381.1:p.Arg348Gly
XM_005271325.2:c.1234A>G XP_005271382.1:p.Arg412Gly
XM_005271326.2:c.1000A>G XP_005271383.1:p.Arg334Gly
XM_005271327.2:c.817A>G XP_005271384.1:p.Arg273Gly
XM_005271322.4:c.1234A>G XP_005271379.1:p.Arg412Gly
XM_005271323.4:c.1192A>G XP_005271380.1:p.Arg398Gly
XM_005271324.5:c.1042A>G XP_005271381.1:p.Arg348Gly
XM_005271325.4:c.1234A>G XP_005271382.1:p.Arg412Gly
XM_005271326.4:c.1000A>G XP_005271383.1:p.Arg334Gly
XM_005271327.4:c.817A>G XP_005271384.1:p.Arg273Gly
NM_001172309.2:c.1042A>G NP_001165780.1:p.Arg348Gly
NM_144573.4:c.1234A>G MANE Select NP_653174.3:p.Arg412Gly