Canonical Allele Identifier: CA1177628328

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935980A= , CM000663.2:g.77935980A=	GRCh38
NC_000001.10:g.78401665A= , CM000663.1:g.78401665A=	GRCh37
NC_000001.9:g.78174253A=	NCBI36
NG_016625.1:g.52466A= , LRG_442:g.52466A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1409A= MANE Select	ENSP00000333938.7:p.Glu470=
ENST00000330010.12:c.1217A=	ENSP00000327363.8:p.Glu406=
ENST00000334785.11:c.1409A=	ENSP00000333938.7:p.Glu470=
ENST00000342754.5:c.1108A=
ENST00000480732.2:n.983A=
NM_001172309.1:c.1217A=	NP_001165780.1:p.Glu406=
NM_144573.3:c.1409A= , LRG_442t1:c.1409A=	NP_653174.3:p.Glu470=
XM_005271322.2:c.1409A=	XP_005271379.1:p.Glu470=
XM_005271323.2:c.1367A=	XP_005271380.1:p.Glu456=
XM_005271324.3:c.1217A=	XP_005271381.1:p.Glu406=
XM_005271325.2:c.1251+2501A=	XP_005271382.1:n.1251+2501A=
XM_005271326.2:c.1175A=	XP_005271383.1:p.Glu392=
XM_005271327.2:c.992A=	XP_005271384.1:p.Glu331=
XM_005271322.4:c.1409A=	XP_005271379.1:p.Glu470=
XM_005271323.4:c.1367A=	XP_005271380.1:p.Glu456=
XM_005271324.5:c.1217A=	XP_005271381.1:p.Glu406=
XM_005271325.4:c.1251+2501A=	XP_005271382.1:n.1251+2501A=
XM_005271326.4:c.1175A=	XP_005271383.1:p.Glu392=
XM_005271327.4:c.992A=	XP_005271384.1:p.Glu331=
NM_001172309.2:c.1217A=	NP_001165780.1:p.Glu406=
NM_144573.4:c.1409A= MANE Select	NP_653174.3:p.Glu470=