Canonical Allele Identifier: CA1177628266

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935829G= , CM000663.2:g.77935829G=	GRCh38
NC_000001.10:g.78401514G= , CM000663.1:g.78401514G=	GRCh37
NC_000001.9:g.78174102G=	NCBI36
NG_016625.1:g.52315G= , LRG_442:g.52315G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1258G= MANE Select	ENSP00000333938.7:p.Glu420=
ENST00000330010.12:c.1066G=	ENSP00000327363.8:p.Glu356=
ENST00000334785.11:c.1258G=	ENSP00000333938.7:p.Glu420=
ENST00000342754.5:c.957G=
ENST00000440324.5:c.1216G=	ENSP00000411902.1:p.Glu406=
ENST00000464998.1:n.718G=
ENST00000480732.2:n.832G=
NM_001172309.1:c.1066G=	NP_001165780.1:p.Glu356=
NM_144573.3:c.1258G= , LRG_442t1:c.1258G=	NP_653174.3:p.Glu420=
XM_005271322.2:c.1258G=	XP_005271379.1:p.Glu420=
XM_005271323.2:c.1216G=	XP_005271380.1:p.Glu406=
XM_005271324.3:c.1066G=	XP_005271381.1:p.Glu356=
XM_005271325.2:c.1251+2350G=	XP_005271382.1:n.1251+2350G=
XM_005271326.2:c.1024G=	XP_005271383.1:p.Glu342=
XM_005271327.2:c.841G=	XP_005271384.1:p.Glu281=
XM_005271322.4:c.1258G=	XP_005271379.1:p.Glu420=
XM_005271323.4:c.1216G=	XP_005271380.1:p.Glu406=
XM_005271324.5:c.1066G=	XP_005271381.1:p.Glu356=
XM_005271325.4:c.1251+2350G=	XP_005271382.1:n.1251+2350G=
XM_005271326.4:c.1024G=	XP_005271383.1:p.Glu342=
XM_005271327.4:c.841G=	XP_005271384.1:p.Glu281=
NM_001172309.2:c.1066G=	NP_001165780.1:p.Glu356=
NM_144573.4:c.1258G= MANE Select	NP_653174.3:p.Glu420=