Canonical Allele Identifier: CA2574414118

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935957_77935958del , CM000663.2:g.77935957_77935958del	GRCh38
NC_000001.10:g.78401642_78401643del , CM000663.1:g.78401642_78401643del	GRCh37
NC_000001.9:g.78174230_78174231del	NCBI36
NG_016625.1:g.52443_52444del , LRG_442:g.52443_52444del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1386_1387del MANE Select	ENSP00000333938.7:p.Glu462AspfsTer16
ENST00000330010.12:c.1194_1195del	ENSP00000327363.8:p.Glu398AspfsTer16
ENST00000334785.11:c.1386_1387del	ENSP00000333938.7:p.Glu462AspfsTer16
ENST00000342754.5:c.1085_1086del
ENST00000464998.1:n.846_847del
ENST00000480732.2:n.960_961del
NM_001172309.1:c.1194_1195del	NP_001165780.1:p.Glu398AspfsTer16
NM_144573.3:c.1386_1387del , LRG_442t1:c.1386_1387del	NP_653174.3:p.Glu462AspfsTer16
XM_005271322.2:c.1386_1387del	XP_005271379.1:p.Glu462AspfsTer16
XM_005271323.2:c.1344_1345del	XP_005271380.1:p.Glu448AspfsTer16
XM_005271324.3:c.1194_1195del	XP_005271381.1:p.Glu398AspfsTer16
XM_005271325.2:c.1251+2478_1251+2479del	XP_005271382.1:n.1251+2478_1251+2479del
XM_005271326.2:c.1152_1153del	XP_005271383.1:p.Glu384AspfsTer16
XM_005271327.2:c.969_970del	XP_005271384.1:p.Glu323AspfsTer16
XM_005271322.4:c.1386_1387del	XP_005271379.1:p.Glu462AspfsTer16
XM_005271323.4:c.1344_1345del	XP_005271380.1:p.Glu448AspfsTer16
XM_005271324.5:c.1194_1195del	XP_005271381.1:p.Glu398AspfsTer16
XM_005271325.4:c.1251+2478_1251+2479del	XP_005271382.1:n.1251+2478_1251+2479del
XM_005271326.4:c.1152_1153del	XP_005271383.1:p.Glu384AspfsTer16
XM_005271327.4:c.969_970del	XP_005271384.1:p.Glu323AspfsTer16
NM_001172309.2:c.1194_1195del	NP_001165780.1:p.Glu398AspfsTer16
NM_144573.4:c.1386_1387del MANE Select	NP_653174.3:p.Glu462AspfsTer16