Canonical Allele Identifier: CA524230677
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs1491169388
gnomAD v2: 1-78383787-ACT-A
gnomAD v4: 1-77918102-ACT-A
MyVariant Identifiers: chr1:g.78383788_78383789del (hg19) chr1:g.77918103_77918104del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77918103_77918104del , CM000663.2:g.77918103_77918104del GRCh38
NC_000001.10:g.78383788_78383789del , CM000663.1:g.78383788_78383789del GRCh37
NC_000001.9:g.78156376_78156377del NCBI36
NG_016625.1:g.34589_34590del , LRG_442:g.34589_34590del

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.299-22_299-21del MANE Select ENSP00000333938.7:n.299-22_299-21del
ENST00000330010.12:c.107-22_107-21del ENSP00000327363.8:n.107-22_107-21del
ENST00000334785.11:c.299-22_299-21del ENSP00000333938.7:n.299-22_299-21del
ENST00000401035.7:c.107-22_107-21del ENSP00000383814.3:n.107-22_107-21del
ENST00000440324.5:c.299-22_299-21del ENSP00000411902.1:n.299-22_299-21del
NM_001172309.1:c.107-22_107-21del NP_001165780.1:n.107-22_107-21del
NM_144573.3:c.299-22_299-21del , LRG_442t1:c.299-22_299-21del NP_653174.3:n.299-22_299-21del
XM_005271322.2:c.299-22_299-21del XP_005271379.1:n.299-22_299-21del
XM_005271323.2:c.299-22_299-21del XP_005271380.1:n.299-22_299-21del
XM_005271324.3:c.107-22_107-21del XP_005271381.1:n.107-22_107-21del
XM_005271325.2:c.299-22_299-21del XP_005271382.1:n.299-22_299-21del
XM_005271326.2:c.107-22_107-21del XP_005271383.1:n.107-22_107-21del
XM_005271327.2:c.299-22_299-21del XP_005271384.1:n.299-22_299-21del
XM_005271322.4:c.299-22_299-21del XP_005271379.1:n.299-22_299-21del
XM_005271323.4:c.299-22_299-21del XP_005271380.1:n.299-22_299-21del
XM_005271324.5:c.107-22_107-21del XP_005271381.1:n.107-22_107-21del
XM_005271325.4:c.299-22_299-21del XP_005271382.1:n.299-22_299-21del
XM_005271326.4:c.107-22_107-21del XP_005271383.1:n.107-22_107-21del
XM_005271327.4:c.299-22_299-21del XP_005271384.1:n.299-22_299-21del
NM_001172309.2:c.107-22_107-21del NP_001165780.1:n.107-22_107-21del
NM_144573.4:c.299-22_299-21del MANE Select NP_653174.3:n.299-22_299-21del
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