Canonical Allele Identifier: CA1143622015

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936024G= , CM000663.2:g.77936024G=	GRCh38
NC_000001.10:g.78401709G= , CM000663.1:g.78401709G=	GRCh37
NC_000001.9:g.78174297G=	NCBI36
NG_016625.1:g.52510G= , LRG_442:g.52510G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1453G= MANE Select	ENSP00000333938.7:p.Glu485=
ENST00000330010.12:c.1261G=	ENSP00000327363.8:p.Glu421=
ENST00000334785.11:c.1453G=	ENSP00000333938.7:p.Glu485=
ENST00000342754.5:c.1152G=
ENST00000480732.2:n.1027G=
NM_001172309.1:c.1261G=	NP_001165780.1:p.Glu421=
NM_144573.3:c.1453G= , LRG_442t1:c.1453G=	NP_653174.3:p.Glu485=
XM_005271322.2:c.1453G=	XP_005271379.1:p.Glu485=
XM_005271323.2:c.1411G=	XP_005271380.1:p.Glu471=
XM_005271324.3:c.1261G=	XP_005271381.1:p.Glu421=
XM_005271325.2:c.1251+2545G=	XP_005271382.1:n.1251+2545G=
XM_005271326.2:c.1219G=	XP_005271383.1:p.Glu407=
XM_005271327.2:c.1036G=	XP_005271384.1:p.Glu346=
XM_005271322.4:c.1453G=	XP_005271379.1:p.Glu485=
XM_005271323.4:c.1411G=	XP_005271380.1:p.Glu471=
XM_005271324.5:c.1261G=	XP_005271381.1:p.Glu421=
XM_005271325.4:c.1251+2545G=	XP_005271382.1:n.1251+2545G=
XM_005271326.4:c.1219G=	XP_005271383.1:p.Glu407=
XM_005271327.4:c.1036G=	XP_005271384.1:p.Glu346=
NM_001172309.2:c.1261G=	NP_001165780.1:p.Glu421=
NM_144573.4:c.1453G= MANE Select	NP_653174.3:p.Glu485=