Canonical Allele Identifier: CA1146530307

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942208G= , CM000663.2:g.77942208G=	GRCh38
NC_000001.10:g.78407893G= , CM000663.1:g.78407893G=	GRCh37
NC_000001.9:g.78180481G=	NCBI36
NG_016625.1:g.58694G= , LRG_442:g.58694G=
NG_033243.2:g.41886C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1659G= MANE Select	ENSP00000333938.7:p.Lys553=
ENST00000330010.12:c.1467G=	ENSP00000327363.8:p.Lys489=
ENST00000334785.11:c.1659G=	ENSP00000333938.7:p.Lys553=
ENST00000342754.5:c.1358G=
ENST00000470735.1:n.498G=
ENST00000480732.2:n.1233G=
NM_001172309.1:c.1467G=	NP_001165780.1:p.Lys489=
NM_144573.3:c.1659G= , LRG_442t1:c.1659G=	NP_653174.3:p.Lys553=
XM_005271322.2:c.1659G=	XP_005271379.1:p.Lys553=
XM_005271323.2:c.1617G=	XP_005271380.1:p.Lys539=
XM_005271324.3:c.1467G=	XP_005271381.1:p.Lys489=
XM_005271325.2:c.1437G=	XP_005271382.1:p.Lys479=
XM_005271326.2:c.1425G=	XP_005271383.1:p.Lys475=
XM_005271327.2:c.1242G=	XP_005271384.1:p.Lys414=
XM_005271322.4:c.1659G=	XP_005271379.1:p.Lys553=
XM_005271323.4:c.1617G=	XP_005271380.1:p.Lys539=
XM_005271324.5:c.1467G=	XP_005271381.1:p.Lys489=
XM_005271325.4:c.1437G=	XP_005271382.1:p.Lys479=
XM_005271326.4:c.1425G=	XP_005271383.1:p.Lys475=
XM_005271327.4:c.1242G=	XP_005271384.1:p.Lys414=
NM_001172309.2:c.1467G=	NP_001165780.1:p.Lys489=
NM_144573.4:c.1659G= MANE Select	NP_653174.3:p.Lys553=