Canonical Allele Identifier: CA1177631145

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942082G= , CM000663.2:g.77942082G=	GRCh38
NC_000001.10:g.78407767G= , CM000663.1:g.78407767G=	GRCh37
NC_000001.9:g.78180355G=	NCBI36
NG_016625.1:g.58568G= , LRG_442:g.58568G=
NG_033243.2:g.42012C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1533G= MANE Select	ENSP00000333938.7:p.Val511=
ENST00000330010.12:c.1341G=	ENSP00000327363.8:p.Val447=
ENST00000334785.11:c.1533G=	ENSP00000333938.7:p.Val511=
ENST00000342754.5:c.1232G=
ENST00000470735.1:n.372G=
ENST00000480732.2:n.1107G=
NM_001172309.1:c.1341G=	NP_001165780.1:p.Val447=
NM_144573.3:c.1533G= , LRG_442t1:c.1533G=	NP_653174.3:p.Val511=
XM_005271322.2:c.1533G=	XP_005271379.1:p.Val511=
XM_005271323.2:c.1491G=	XP_005271380.1:p.Val497=
XM_005271324.3:c.1341G=	XP_005271381.1:p.Val447=
XM_005271325.2:c.1311G=	XP_005271382.1:p.Val437=
XM_005271326.2:c.1299G=	XP_005271383.1:p.Val433=
XM_005271327.2:c.1116G=	XP_005271384.1:p.Val372=
XM_005271322.4:c.1533G=	XP_005271379.1:p.Val511=
XM_005271323.4:c.1491G=	XP_005271380.1:p.Val497=
XM_005271324.5:c.1341G=	XP_005271381.1:p.Val447=
XM_005271325.4:c.1311G=	XP_005271382.1:p.Val437=
XM_005271326.4:c.1299G=	XP_005271383.1:p.Val433=
XM_005271327.4:c.1116G=	XP_005271384.1:p.Val372=
NM_001172309.2:c.1341G=	NP_001165780.1:p.Val447=
NM_144573.4:c.1533G= MANE Select	NP_653174.3:p.Val511=