Canonical Allele Identifier: CA918627

Gene: NEXN

Linked Data

• ClinVar Variation Id: 1575405
• ClinVar RCV Id: RCV002075091
• dbSNP Id: rs773500471
• ExAC: 1:78383884 C / A
• gnomAD v2: 1-78383884-C-A
• gnomAD v4: 1-77918199-C-A
• MyVariant Identifiers: chr1:g.78383884C>A (hg19) ; chr1:g.77918199C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77918199C>A , CM000663.2:g.77918199C>A	GRCh38
NC_000001.10:g.78383884C>A , CM000663.1:g.78383884C>A	GRCh37
NC_000001.9:g.78156472C>A	NCBI36
NG_016625.1:g.34685C>A , LRG_442:g.34685C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.373C>A MANE Select	ENSP00000333938.7:p.Arg125=
ENST00000330010.12:c.181C>A	ENSP00000327363.8:p.Arg61=
ENST00000334785.11:c.373C>A	ENSP00000333938.7:p.Arg125=
ENST00000342754.5:c.72C>A
ENST00000401035.7:c.181C>A	ENSP00000383814.3:p.Arg61=
ENST00000440324.5:c.373C>A	ENSP00000411902.1:p.Arg125=
NM_001172309.1:c.181C>A	NP_001165780.1:p.Arg61=
NM_144573.3:c.373C>A , LRG_442t1:c.373C>A	NP_653174.3:p.Arg125=
XM_005271322.2:c.373C>A	XP_005271379.1:p.Arg125=
XM_005271323.2:c.373C>A	XP_005271380.1:p.Arg125=
XM_005271324.3:c.181C>A	XP_005271381.1:p.Arg61=
XM_005271325.2:c.373C>A	XP_005271382.1:p.Arg125=
XM_005271326.2:c.181C>A	XP_005271383.1:p.Arg61=
XM_005271327.2:c.373C>A	XP_005271384.1:p.Arg125=
XM_005271322.4:c.373C>A	XP_005271379.1:p.Arg125=
XM_005271323.4:c.373C>A	XP_005271380.1:p.Arg125=
XM_005271324.5:c.181C>A	XP_005271381.1:p.Arg61=
XM_005271325.4:c.373C>A	XP_005271382.1:p.Arg125=
XM_005271326.4:c.181C>A	XP_005271383.1:p.Arg61=
XM_005271327.4:c.373C>A	XP_005271384.1:p.Arg125=
NM_001172309.2:c.181C>A	NP_001165780.1:p.Arg61=
NM_144573.4:c.373C>A MANE Select	NP_653174.3:p.Arg125=