Canonical Allele Identifier: CA1143959920

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935985G= , CM000663.2:g.77935985G=	GRCh38
NC_000001.10:g.78401670G= , CM000663.1:g.78401670G=	GRCh37
NC_000001.9:g.78174258G=	NCBI36
NG_016625.1:g.52471G= , LRG_442:g.52471G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1414G= MANE Select	ENSP00000333938.7:p.Ala472=
ENST00000330010.12:c.1222G=	ENSP00000327363.8:p.Ala408=
ENST00000334785.11:c.1414G=	ENSP00000333938.7:p.Ala472=
ENST00000342754.5:c.1113G=
ENST00000480732.2:n.988G=
NM_001172309.1:c.1222G=	NP_001165780.1:p.Ala408=
NM_144573.3:c.1414G= , LRG_442t1:c.1414G=	NP_653174.3:p.Ala472=
XM_005271322.2:c.1414G=	XP_005271379.1:p.Ala472=
XM_005271323.2:c.1372G=	XP_005271380.1:p.Ala458=
XM_005271324.3:c.1222G=	XP_005271381.1:p.Ala408=
XM_005271325.2:c.1251+2506G=	XP_005271382.1:n.1251+2506G=
XM_005271326.2:c.1180G=	XP_005271383.1:p.Ala394=
XM_005271327.2:c.997G=	XP_005271384.1:p.Ala333=
XM_005271322.4:c.1414G=	XP_005271379.1:p.Ala472=
XM_005271323.4:c.1372G=	XP_005271380.1:p.Ala458=
XM_005271324.5:c.1222G=	XP_005271381.1:p.Ala408=
XM_005271325.4:c.1251+2506G=	XP_005271382.1:n.1251+2506G=
XM_005271326.4:c.1180G=	XP_005271383.1:p.Ala394=
XM_005271327.4:c.997G=	XP_005271384.1:p.Ala333=
NM_001172309.2:c.1222G=	NP_001165780.1:p.Ala408=
NM_144573.4:c.1414G= MANE Select	NP_653174.3:p.Ala472=