Canonical Allele Identifier: CA1177626332

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942911T= , CM000663.2:g.77942911T=	GRCh38
NC_000001.10:g.78408596T= , CM000663.1:g.78408596T=	GRCh37
NC_000001.9:g.78181184T=	NCBI36
NG_016625.1:g.59397T= , LRG_442:g.59397T=
NG_033243.2:g.41183A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*82T= MANE Select	ENSP00000333938.7:n.*82T=
ENST00000330010.12:c.*82T=	ENSP00000327363.8:n.*82T=
ENST00000334785.11:c.*82T=	ENSP00000333938.7:n.*82T=
ENST00000342754.5:c.1728T=
ENST00000480732.2:n.1684T=
NM_001172309.1:c.*82T=	NP_001165780.1:n.*82T=
NM_144573.3:c.*82T= , LRG_442t1:c.*82T=	NP_653174.3:n.*82T=
XM_005271322.2:c.2029T=	XP_005271379.1:p.Ter677=
XM_005271323.2:c.1987T=	XP_005271380.1:p.Ter663=
XM_005271324.3:c.1837T=	XP_005271381.1:p.Ter613=
XM_005271325.2:c.1807T=	XP_005271382.1:p.Ter603=
XM_005271326.2:c.1795T=	XP_005271383.1:p.Ter599=
XM_005271327.2:c.1612T=	XP_005271384.1:p.Ter538=
XM_005271322.4:c.2029T=	XP_005271379.1:p.Ter677=
XM_005271323.4:c.1987T=	XP_005271380.1:p.Ter663=
XM_005271324.5:c.1837T=	XP_005271381.1:p.Ter613=
XM_005271325.4:c.1807T=	XP_005271382.1:p.Ter603=
XM_005271326.4:c.1795T=	XP_005271383.1:p.Ter599=
XM_005271327.4:c.1612T=	XP_005271384.1:p.Ter538=
NM_001172309.2:c.*82T=	NP_001165780.1:n.*82T=
NM_144573.4:c.*82T= MANE Select	NP_653174.3:n.*82T=