Canonical Allele Identifier: CA1143393217

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942131G= , CM000663.2:g.77942131G=	GRCh38
NC_000001.10:g.78407816G= , CM000663.1:g.78407816G=	GRCh37
NC_000001.9:g.78180404G=	NCBI36
NG_016625.1:g.58617G= , LRG_442:g.58617G=
NG_033243.2:g.41963C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1582G= MANE Select	ENSP00000333938.7:p.Glu528=
ENST00000330010.12:c.1390G=	ENSP00000327363.8:p.Glu464=
ENST00000334785.11:c.1582G=	ENSP00000333938.7:p.Glu528=
ENST00000342754.5:c.1281G=
ENST00000470735.1:n.421G=
ENST00000480732.2:n.1156G=
NM_001172309.1:c.1390G=	NP_001165780.1:p.Glu464=
NM_144573.3:c.1582G= , LRG_442t1:c.1582G=	NP_653174.3:p.Glu528=
XM_005271322.2:c.1582G=	XP_005271379.1:p.Glu528=
XM_005271323.2:c.1540G=	XP_005271380.1:p.Glu514=
XM_005271324.3:c.1390G=	XP_005271381.1:p.Glu464=
XM_005271325.2:c.1360G=	XP_005271382.1:p.Glu454=
XM_005271326.2:c.1348G=	XP_005271383.1:p.Glu450=
XM_005271327.2:c.1165G=	XP_005271384.1:p.Glu389=
XM_005271322.4:c.1582G=	XP_005271379.1:p.Glu528=
XM_005271323.4:c.1540G=	XP_005271380.1:p.Glu514=
XM_005271324.5:c.1390G=	XP_005271381.1:p.Glu464=
XM_005271325.4:c.1360G=	XP_005271382.1:p.Glu454=
XM_005271326.4:c.1348G=	XP_005271383.1:p.Glu450=
XM_005271327.4:c.1165G=	XP_005271384.1:p.Glu389=
NM_001172309.2:c.1390G=	NP_001165780.1:p.Glu464=
NM_144573.4:c.1582G= MANE Select	NP_653174.3:p.Glu528=