Canonical Allele Identifier: CA340881099

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407801G>A (hg19) ; chr1:g.77942116G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942116G>A , CM000663.2:g.77942116G>A	GRCh38
NC_000001.10:g.78407801G>A , CM000663.1:g.78407801G>A	GRCh37
NC_000001.9:g.78180389G>A	NCBI36
NG_016625.1:g.58602G>A , LRG_442:g.58602G>A
NG_033243.2:g.41978C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1567G>A MANE Select	ENSP00000333938.7:p.Ala523Thr
ENST00000330010.12:c.1375G>A	ENSP00000327363.8:p.Ala459Thr
ENST00000334785.11:c.1567G>A	ENSP00000333938.7:p.Ala523Thr
ENST00000342754.5:c.1266G>A
ENST00000470735.1:n.406G>A
ENST00000480732.2:n.1141G>A
NM_001172309.1:c.1375G>A	NP_001165780.1:p.Ala459Thr
NM_144573.3:c.1567G>A , LRG_442t1:c.1567G>A	NP_653174.3:p.Ala523Thr
XM_005271322.2:c.1567G>A	XP_005271379.1:p.Ala523Thr
XM_005271323.2:c.1525G>A	XP_005271380.1:p.Ala509Thr
XM_005271324.3:c.1375G>A	XP_005271381.1:p.Ala459Thr
XM_005271325.2:c.1345G>A	XP_005271382.1:p.Ala449Thr
XM_005271326.2:c.1333G>A	XP_005271383.1:p.Ala445Thr
XM_005271327.2:c.1150G>A	XP_005271384.1:p.Ala384Thr
XM_005271322.4:c.1567G>A	XP_005271379.1:p.Ala523Thr
XM_005271323.4:c.1525G>A	XP_005271380.1:p.Ala509Thr
XM_005271324.5:c.1375G>A	XP_005271381.1:p.Ala459Thr
XM_005271325.4:c.1345G>A	XP_005271382.1:p.Ala449Thr
XM_005271326.4:c.1333G>A	XP_005271383.1:p.Ala445Thr
XM_005271327.4:c.1150G>A	XP_005271384.1:p.Ala384Thr
NM_001172309.2:c.1375G>A	NP_001165780.1:p.Ala459Thr
NM_144573.4:c.1567G>A MANE Select	NP_653174.3:p.Ala523Thr