Canonical Allele Identifier: CA919004

Gene: NEXN

Linked Data

• ClinVar Variation Id: 1584821
• ClinVar RCV Id: RCV002102875 ; RCV004045796
• dbSNP Id: rs374467054
• ExAC: 1:78408385 G / A
• gnomAD v2: 1-78408385-G-A
• gnomAD v3: 1-77942700-G-A
• gnomAD v4: 1-77942700-G-A
• MyVariant Identifiers: chr1:g.78408385G>A (hg19) ; chr1:g.77942700G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942700G>A , CM000663.2:g.77942700G>A	GRCh38
NC_000001.10:g.78408385G>A , CM000663.1:g.78408385G>A	GRCh37
NC_000001.9:g.78180973G>A	NCBI36
NG_016625.1:g.59186G>A , LRG_442:g.59186G>A
NG_033243.2:g.41394C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1899G>A MANE Select	ENSP00000333938.7:p.Arg633=
ENST00000330010.12:c.1707G>A	ENSP00000327363.8:p.Arg569=
ENST00000334785.11:c.1899G>A	ENSP00000333938.7:p.Arg633=
ENST00000342754.5:c.1598G>A
ENST00000470735.1:n.738G>A
ENST00000480732.2:n.1473G>A
NM_001172309.1:c.1707G>A	NP_001165780.1:p.Arg569=
NM_144573.3:c.1899G>A , LRG_442t1:c.1899G>A	NP_653174.3:p.Arg633=
XM_005271322.2:c.1899G>A	XP_005271379.1:p.Arg633=
XM_005271323.2:c.1857G>A	XP_005271380.1:p.Arg619=
XM_005271324.3:c.1707G>A	XP_005271381.1:p.Arg569=
XM_005271325.2:c.1677G>A	XP_005271382.1:p.Arg559=
XM_005271326.2:c.1665G>A	XP_005271383.1:p.Arg555=
XM_005271327.2:c.1482G>A	XP_005271384.1:p.Arg494=
XM_005271322.4:c.1899G>A	XP_005271379.1:p.Arg633=
XM_005271323.4:c.1857G>A	XP_005271380.1:p.Arg619=
XM_005271324.5:c.1707G>A	XP_005271381.1:p.Arg569=
XM_005271325.4:c.1677G>A	XP_005271382.1:p.Arg559=
XM_005271326.4:c.1665G>A	XP_005271383.1:p.Arg555=
XM_005271327.4:c.1482G>A	XP_005271384.1:p.Arg494=
NM_001172309.2:c.1707G>A	NP_001165780.1:p.Arg569=
NM_144573.4:c.1899G>A MANE Select	NP_653174.3:p.Arg633=