Canonical Allele Identifier: CA1143965877

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942797A= , CM000663.2:g.77942797A=	GRCh38
NC_000001.10:g.78408482A= , CM000663.1:g.78408482A=	GRCh37
NC_000001.9:g.78181070A=	NCBI36
NG_016625.1:g.59283A= , LRG_442:g.59283A=
NG_033243.2:g.41297T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1996A= MANE Select	ENSP00000333938.7:p.Thr666=
ENST00000330010.12:c.1804A=	ENSP00000327363.8:p.Thr602=
ENST00000334785.11:c.1996A=	ENSP00000333938.7:p.Thr666=
ENST00000342754.5:c.1695A=
ENST00000480732.2:n.1570A=
NM_001172309.1:c.1804A=	NP_001165780.1:p.Thr602=
NM_144573.3:c.1996A= , LRG_442t1:c.1996A=	NP_653174.3:p.Thr666=
XM_005271322.2:c.1996A=	XP_005271379.1:p.Thr666=
XM_005271323.2:c.1954A=	XP_005271380.1:p.Thr652=
XM_005271324.3:c.1804A=	XP_005271381.1:p.Thr602=
XM_005271325.2:c.1774A=	XP_005271382.1:p.Thr592=
XM_005271326.2:c.1762A=	XP_005271383.1:p.Thr588=
XM_005271327.2:c.1579A=	XP_005271384.1:p.Thr527=
XM_005271322.4:c.1996A=	XP_005271379.1:p.Thr666=
XM_005271323.4:c.1954A=	XP_005271380.1:p.Thr652=
XM_005271324.5:c.1804A=	XP_005271381.1:p.Thr602=
XM_005271325.4:c.1774A=	XP_005271382.1:p.Thr592=
XM_005271326.4:c.1762A=	XP_005271383.1:p.Thr588=
XM_005271327.4:c.1579A=	XP_005271384.1:p.Thr527=
NM_001172309.2:c.1804A=	NP_001165780.1:p.Thr602=
NM_144573.4:c.1996A= MANE Select	NP_653174.3:p.Thr666=