Canonical Allele Identifier: CA1177631162

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942122G= , CM000663.2:g.77942122G=	GRCh38
NC_000001.10:g.78407807G= , CM000663.1:g.78407807G=	GRCh37
NC_000001.9:g.78180395G=	NCBI36
NG_016625.1:g.58608G= , LRG_442:g.58608G=
NG_033243.2:g.41972C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1573G= MANE Select	ENSP00000333938.7:p.Glu525=
ENST00000330010.12:c.1381G=	ENSP00000327363.8:p.Glu461=
ENST00000334785.11:c.1573G=	ENSP00000333938.7:p.Glu525=
ENST00000342754.5:c.1272G=
ENST00000470735.1:n.412G=
ENST00000480732.2:n.1147G=
NM_001172309.1:c.1381G=	NP_001165780.1:p.Glu461=
NM_144573.3:c.1573G= , LRG_442t1:c.1573G=	NP_653174.3:p.Glu525=
XM_005271322.2:c.1573G=	XP_005271379.1:p.Glu525=
XM_005271323.2:c.1531G=	XP_005271380.1:p.Glu511=
XM_005271324.3:c.1381G=	XP_005271381.1:p.Glu461=
XM_005271325.2:c.1351G=	XP_005271382.1:p.Glu451=
XM_005271326.2:c.1339G=	XP_005271383.1:p.Glu447=
XM_005271327.2:c.1156G=	XP_005271384.1:p.Glu386=
XM_005271322.4:c.1573G=	XP_005271379.1:p.Glu525=
XM_005271323.4:c.1531G=	XP_005271380.1:p.Glu511=
XM_005271324.5:c.1381G=	XP_005271381.1:p.Glu461=
XM_005271325.4:c.1351G=	XP_005271382.1:p.Glu451=
XM_005271326.4:c.1339G=	XP_005271383.1:p.Glu447=
XM_005271327.4:c.1156G=	XP_005271384.1:p.Glu386=
NM_001172309.2:c.1381G=	NP_001165780.1:p.Glu461=
NM_144573.4:c.1573G= MANE Select	NP_653174.3:p.Glu525=