Canonical Allele Identifier: CA1177626678

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933299C= , CM000663.2:g.77933299C=	GRCh38
NC_000001.10:g.78398984C= , CM000663.1:g.78398984C=	GRCh37
NC_000001.9:g.78171572C=	NCBI36
NG_016625.1:g.49785C= , LRG_442:g.49785C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1071C= MANE Select	ENSP00000333938.7:p.Ser357=
ENST00000330010.12:c.879C=	ENSP00000327363.8:p.Ser293=
ENST00000334785.11:c.1071C=	ENSP00000333938.7:p.Ser357=
ENST00000342754.5:c.770C=
ENST00000401035.7:c.879C=	ENSP00000383814.3:p.Ser293=
ENST00000440324.5:c.1029C=	ENSP00000411902.1:p.Ser343=
ENST00000464998.1:n.531C=
ENST00000480732.2:n.645C=
NM_001172309.1:c.879C=	NP_001165780.1:p.Ser293=
NM_144573.3:c.1071C= , LRG_442t1:c.1071C=	NP_653174.3:p.Ser357=
XM_005271322.2:c.1071C=	XP_005271379.1:p.Ser357=
XM_005271323.2:c.1029C=	XP_005271380.1:p.Ser343=
XM_005271324.3:c.879C=	XP_005271381.1:p.Ser293=
XM_005271325.2:c.1071C=	XP_005271382.1:p.Ser357=
XM_005271326.2:c.837C=	XP_005271383.1:p.Ser279=
XM_005271327.2:c.654C=	XP_005271384.1:p.Ser218=
XM_005271322.4:c.1071C=	XP_005271379.1:p.Ser357=
XM_005271323.4:c.1029C=	XP_005271380.1:p.Ser343=
XM_005271324.5:c.879C=	XP_005271381.1:p.Ser293=
XM_005271325.4:c.1071C=	XP_005271382.1:p.Ser357=
XM_005271326.4:c.837C=	XP_005271383.1:p.Ser279=
XM_005271327.4:c.654C=	XP_005271384.1:p.Ser218=
NM_001172309.2:c.879C=	NP_001165780.1:p.Ser293=
NM_144573.4:c.1071C= MANE Select	NP_653174.3:p.Ser357=