Canonical Allele Identifier: CA1148277138

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942133A= , CM000663.2:g.77942133A=	GRCh38
NC_000001.10:g.78407818A= , CM000663.1:g.78407818A=	GRCh37
NC_000001.9:g.78180406A=	NCBI36
NG_016625.1:g.58619A= , LRG_442:g.58619A=
NG_033243.2:g.41961T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1584A= MANE Select	ENSP00000333938.7:p.Glu528=
ENST00000330010.12:c.1392A=	ENSP00000327363.8:p.Glu464=
ENST00000334785.11:c.1584A=	ENSP00000333938.7:p.Glu528=
ENST00000342754.5:c.1283A=
ENST00000470735.1:n.423A=
ENST00000480732.2:n.1158A=
NM_001172309.1:c.1392A=	NP_001165780.1:p.Glu464=
NM_144573.3:c.1584A= , LRG_442t1:c.1584A=	NP_653174.3:p.Glu528=
XM_005271322.2:c.1584A=	XP_005271379.1:p.Glu528=
XM_005271323.2:c.1542A=	XP_005271380.1:p.Glu514=
XM_005271324.3:c.1392A=	XP_005271381.1:p.Glu464=
XM_005271325.2:c.1362A=	XP_005271382.1:p.Glu454=
XM_005271326.2:c.1350A=	XP_005271383.1:p.Glu450=
XM_005271327.2:c.1167A=	XP_005271384.1:p.Glu389=
XM_005271322.4:c.1584A=	XP_005271379.1:p.Glu528=
XM_005271323.4:c.1542A=	XP_005271380.1:p.Glu514=
XM_005271324.5:c.1392A=	XP_005271381.1:p.Glu464=
XM_005271325.4:c.1362A=	XP_005271382.1:p.Glu454=
XM_005271326.4:c.1350A=	XP_005271383.1:p.Glu450=
XM_005271327.4:c.1167A=	XP_005271384.1:p.Glu389=
NM_001172309.2:c.1392A=	NP_001165780.1:p.Glu464=
NM_144573.4:c.1584A= MANE Select	NP_653174.3:p.Glu528=