Canonical Allele Identifier: CA1177631477

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942801G= , CM000663.2:g.77942801G=	GRCh38
NC_000001.10:g.78408486G= , CM000663.1:g.78408486G=	GRCh37
NC_000001.9:g.78181074G=	NCBI36
NG_016625.1:g.59287G= , LRG_442:g.59287G=
NG_033243.2:g.41293C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.2000G= MANE Select	ENSP00000333938.7:p.Cys667=
ENST00000330010.12:c.1808G=	ENSP00000327363.8:p.Cys603=
ENST00000334785.11:c.2000G=	ENSP00000333938.7:p.Cys667=
ENST00000342754.5:c.1699G=
ENST00000480732.2:n.1574G=
NM_001172309.1:c.1808G=	NP_001165780.1:p.Cys603=
NM_144573.3:c.2000G= , LRG_442t1:c.2000G=	NP_653174.3:p.Cys667=
XM_005271322.2:c.2000G=	XP_005271379.1:p.Cys667=
XM_005271323.2:c.1958G=	XP_005271380.1:p.Cys653=
XM_005271324.3:c.1808G=	XP_005271381.1:p.Cys603=
XM_005271325.2:c.1778G=	XP_005271382.1:p.Cys593=
XM_005271326.2:c.1766G=	XP_005271383.1:p.Cys589=
XM_005271327.2:c.1583G=	XP_005271384.1:p.Cys528=
XM_005271322.4:c.2000G=	XP_005271379.1:p.Cys667=
XM_005271323.4:c.1958G=	XP_005271380.1:p.Cys653=
XM_005271324.5:c.1808G=	XP_005271381.1:p.Cys603=
XM_005271325.4:c.1778G=	XP_005271382.1:p.Cys593=
XM_005271326.4:c.1766G=	XP_005271383.1:p.Cys589=
XM_005271327.4:c.1583G=	XP_005271384.1:p.Cys528=
NM_001172309.2:c.1808G=	NP_001165780.1:p.Cys603=
NM_144573.4:c.2000G= MANE Select	NP_653174.3:p.Cys667=