Canonical Allele Identifier: CA1140555170

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77918189G= , CM000663.2:g.77918189G=	GRCh38
NC_000001.10:g.78383874G= , CM000663.1:g.78383874G=	GRCh37
NC_000001.9:g.78156462G=	NCBI36
NG_016625.1:g.34675G= , LRG_442:g.34675G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.363G= MANE Select	ENSP00000333938.7:p.Thr121=
ENST00000330010.12:c.171G=	ENSP00000327363.8:p.Thr57=
ENST00000334785.11:c.363G=	ENSP00000333938.7:p.Thr121=
ENST00000342754.5:c.62G=
ENST00000401035.7:c.171G=	ENSP00000383814.3:p.Thr57=
ENST00000440324.5:c.363G=	ENSP00000411902.1:p.Thr121=
NM_001172309.1:c.171G=	NP_001165780.1:p.Thr57=
NM_144573.3:c.363G= , LRG_442t1:c.363G=	NP_653174.3:p.Thr121=
XM_005271322.2:c.363G=	XP_005271379.1:p.Thr121=
XM_005271323.2:c.363G=	XP_005271380.1:p.Thr121=
XM_005271324.3:c.171G=	XP_005271381.1:p.Thr57=
XM_005271325.2:c.363G=	XP_005271382.1:p.Thr121=
XM_005271326.2:c.171G=	XP_005271383.1:p.Thr57=
XM_005271327.2:c.363G=	XP_005271384.1:p.Thr121=
XM_005271322.4:c.363G=	XP_005271379.1:p.Thr121=
XM_005271323.4:c.363G=	XP_005271380.1:p.Thr121=
XM_005271324.5:c.171G=	XP_005271381.1:p.Thr57=
XM_005271325.4:c.363G=	XP_005271382.1:p.Thr121=
XM_005271326.4:c.171G=	XP_005271383.1:p.Thr57=
XM_005271327.4:c.363G=	XP_005271384.1:p.Thr121=
NM_001172309.2:c.171G=	NP_001165780.1:p.Thr57=
NM_144573.4:c.363G= MANE Select	NP_653174.3:p.Thr121=