Canonical Allele Identifier: CA1177628311

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935945G= , CM000663.2:g.77935945G=	GRCh38
NC_000001.10:g.78401630G= , CM000663.1:g.78401630G=	GRCh37
NC_000001.9:g.78174218G=	NCBI36
NG_016625.1:g.52431G= , LRG_442:g.52431G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1374G= MANE Select	ENSP00000333938.7:p.Leu458=
ENST00000330010.12:c.1182G=	ENSP00000327363.8:p.Leu394=
ENST00000334785.11:c.1374G=	ENSP00000333938.7:p.Leu458=
ENST00000342754.5:c.1073G=
ENST00000464998.1:n.834G=
ENST00000480732.2:n.948G=
NM_001172309.1:c.1182G=	NP_001165780.1:p.Leu394=
NM_144573.3:c.1374G= , LRG_442t1:c.1374G=	NP_653174.3:p.Leu458=
XM_005271322.2:c.1374G=	XP_005271379.1:p.Leu458=
XM_005271323.2:c.1332G=	XP_005271380.1:p.Leu444=
XM_005271324.3:c.1182G=	XP_005271381.1:p.Leu394=
XM_005271325.2:c.1251+2466G=	XP_005271382.1:n.1251+2466G=
XM_005271326.2:c.1140G=	XP_005271383.1:p.Leu380=
XM_005271327.2:c.957G=	XP_005271384.1:p.Leu319=
XM_005271322.4:c.1374G=	XP_005271379.1:p.Leu458=
XM_005271323.4:c.1332G=	XP_005271380.1:p.Leu444=
XM_005271324.5:c.1182G=	XP_005271381.1:p.Leu394=
XM_005271325.4:c.1251+2466G=	XP_005271382.1:n.1251+2466G=
XM_005271326.4:c.1140G=	XP_005271383.1:p.Leu380=
XM_005271327.4:c.957G=	XP_005271384.1:p.Leu319=
NM_001172309.2:c.1182G=	NP_001165780.1:p.Leu394=
NM_144573.4:c.1374G= MANE Select	NP_653174.3:p.Leu458=