Canonical Allele Identifier: CA1177631431

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942675G= , CM000663.2:g.77942675G=	GRCh38
NC_000001.10:g.78408360G= , CM000663.1:g.78408360G=	GRCh37
NC_000001.9:g.78180948G=	NCBI36
NG_016625.1:g.59161G= , LRG_442:g.59161G=
NG_033243.2:g.41419C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1874G= MANE Select	ENSP00000333938.7:p.Gly625=
ENST00000330010.12:c.1682G=	ENSP00000327363.8:p.Gly561=
ENST00000334785.11:c.1874G=	ENSP00000333938.7:p.Gly625=
ENST00000342754.5:c.1573G=
ENST00000470735.1:n.713G=
ENST00000480732.2:n.1448G=
NM_001172309.1:c.1682G=	NP_001165780.1:p.Gly561=
NM_144573.3:c.1874G= , LRG_442t1:c.1874G=	NP_653174.3:p.Gly625=
XM_005271322.2:c.1874G=	XP_005271379.1:p.Gly625=
XM_005271323.2:c.1832G=	XP_005271380.1:p.Gly611=
XM_005271324.3:c.1682G=	XP_005271381.1:p.Gly561=
XM_005271325.2:c.1652G=	XP_005271382.1:p.Gly551=
XM_005271326.2:c.1640G=	XP_005271383.1:p.Gly547=
XM_005271327.2:c.1457G=	XP_005271384.1:p.Gly486=
XM_005271322.4:c.1874G=	XP_005271379.1:p.Gly625=
XM_005271323.4:c.1832G=	XP_005271380.1:p.Gly611=
XM_005271324.5:c.1682G=	XP_005271381.1:p.Gly561=
XM_005271325.4:c.1652G=	XP_005271382.1:p.Gly551=
XM_005271326.4:c.1640G=	XP_005271383.1:p.Gly547=
XM_005271327.4:c.1457G=	XP_005271384.1:p.Gly486=
NM_001172309.2:c.1682G=	NP_001165780.1:p.Gly561=
NM_144573.4:c.1874G= MANE Select	NP_653174.3:p.Gly625=