Canonical Allele Identifier: CA1148723744

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935831A= , CM000663.2:g.77935831A=	GRCh38
NC_000001.10:g.78401516A= , CM000663.1:g.78401516A=	GRCh37
NC_000001.9:g.78174104A=	NCBI36
NG_016625.1:g.52317A= , LRG_442:g.52317A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1260A= MANE Select	ENSP00000333938.7:p.Glu420=
ENST00000330010.12:c.1068A=	ENSP00000327363.8:p.Glu356=
ENST00000334785.11:c.1260A=	ENSP00000333938.7:p.Glu420=
ENST00000342754.5:c.959A=
ENST00000440324.5:c.1218A=	ENSP00000411902.1:p.Glu406=
ENST00000464998.1:n.720A=
ENST00000480732.2:n.834A=
NM_001172309.1:c.1068A=	NP_001165780.1:p.Glu356=
NM_144573.3:c.1260A= , LRG_442t1:c.1260A=	NP_653174.3:p.Glu420=
XM_005271322.2:c.1260A=	XP_005271379.1:p.Glu420=
XM_005271323.2:c.1218A=	XP_005271380.1:p.Glu406=
XM_005271324.3:c.1068A=	XP_005271381.1:p.Glu356=
XM_005271325.2:c.1251+2352A=	XP_005271382.1:n.1251+2352A=
XM_005271326.2:c.1026A=	XP_005271383.1:p.Glu342=
XM_005271327.2:c.843A=	XP_005271384.1:p.Glu281=
XM_005271322.4:c.1260A=	XP_005271379.1:p.Glu420=
XM_005271323.4:c.1218A=	XP_005271380.1:p.Glu406=
XM_005271324.5:c.1068A=	XP_005271381.1:p.Glu356=
XM_005271325.4:c.1251+2352A=	XP_005271382.1:n.1251+2352A=
XM_005271326.4:c.1026A=	XP_005271383.1:p.Glu342=
XM_005271327.4:c.843A=	XP_005271384.1:p.Glu281=
NM_001172309.2:c.1068A=	NP_001165780.1:p.Glu356=
NM_144573.4:c.1260A= MANE Select	NP_653174.3:p.Glu420=