Canonical Allele Identifier: CA1177628336

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935997G= , CM000663.2:g.77935997G=	GRCh38
NC_000001.10:g.78401682G= , CM000663.1:g.78401682G=	GRCh37
NC_000001.9:g.78174270G=	NCBI36
NG_016625.1:g.52483G= , LRG_442:g.52483G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1426G= MANE Select	ENSP00000333938.7:p.Ala476=
ENST00000330010.12:c.1234G=	ENSP00000327363.8:p.Ala412=
ENST00000334785.11:c.1426G=	ENSP00000333938.7:p.Ala476=
ENST00000342754.5:c.1125G=
ENST00000480732.2:n.1000G=
NM_001172309.1:c.1234G=	NP_001165780.1:p.Ala412=
NM_144573.3:c.1426G= , LRG_442t1:c.1426G=	NP_653174.3:p.Ala476=
XM_005271322.2:c.1426G=	XP_005271379.1:p.Ala476=
XM_005271323.2:c.1384G=	XP_005271380.1:p.Ala462=
XM_005271324.3:c.1234G=	XP_005271381.1:p.Ala412=
XM_005271325.2:c.1251+2518G=	XP_005271382.1:n.1251+2518G=
XM_005271326.2:c.1192G=	XP_005271383.1:p.Ala398=
XM_005271327.2:c.1009G=	XP_005271384.1:p.Ala337=
XM_005271322.4:c.1426G=	XP_005271379.1:p.Ala476=
XM_005271323.4:c.1384G=	XP_005271380.1:p.Ala462=
XM_005271324.5:c.1234G=	XP_005271381.1:p.Ala412=
XM_005271325.4:c.1251+2518G=	XP_005271382.1:n.1251+2518G=
XM_005271326.4:c.1192G=	XP_005271383.1:p.Ala398=
XM_005271327.4:c.1009G=	XP_005271384.1:p.Ala337=
NM_001172309.2:c.1234G=	NP_001165780.1:p.Ala412=
NM_144573.4:c.1426G= MANE Select	NP_653174.3:p.Ala476=