Canonical Allele Identifier: CA2580652576

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935892_77935893del , CM000663.2:g.77935892_77935893del	GRCh38
NC_000001.10:g.78401577_78401578del , CM000663.1:g.78401577_78401578del	GRCh37
NC_000001.9:g.78174165_78174166del	NCBI36
NG_016625.1:g.52378_52379del , LRG_442:g.52378_52379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1321_1322del MANE Select	ENSP00000333938.7:p.Gly441LeufsTer5
ENST00000330010.12:c.1129_1130del	ENSP00000327363.8:p.Gly377LeufsTer5
ENST00000334785.11:c.1321_1322del	ENSP00000333938.7:p.Gly441LeufsTer5
ENST00000342754.5:c.1020_1021del
ENST00000440324.5:c.1279_1280del	ENSP00000411902.1:p.Gly427LeufsTer5
ENST00000464998.1:n.781_782del
ENST00000480732.2:n.895_896del
NM_001172309.1:c.1129_1130del	NP_001165780.1:p.Gly377LeufsTer5
NM_144573.3:c.1321_1322del , LRG_442t1:c.1321_1322del	NP_653174.3:p.Gly441LeufsTer5
XM_005271322.2:c.1321_1322del	XP_005271379.1:p.Gly441LeufsTer5
XM_005271323.2:c.1279_1280del	XP_005271380.1:p.Gly427LeufsTer5
XM_005271324.3:c.1129_1130del	XP_005271381.1:p.Gly377LeufsTer5
XM_005271325.2:c.1251+2413_1251+2414del	XP_005271382.1:n.1251+2413_1251+2414del
XM_005271326.2:c.1087_1088del	XP_005271383.1:p.Gly363LeufsTer5
XM_005271327.2:c.904_905del	XP_005271384.1:p.Gly302LeufsTer5
XM_005271322.4:c.1321_1322del	XP_005271379.1:p.Gly441LeufsTer5
XM_005271323.4:c.1279_1280del	XP_005271380.1:p.Gly427LeufsTer5
XM_005271324.5:c.1129_1130del	XP_005271381.1:p.Gly377LeufsTer5
XM_005271325.4:c.1251+2413_1251+2414del	XP_005271382.1:n.1251+2413_1251+2414del
XM_005271326.4:c.1087_1088del	XP_005271383.1:p.Gly363LeufsTer5
XM_005271327.4:c.904_905del	XP_005271384.1:p.Gly302LeufsTer5
NM_001172309.2:c.1129_1130del	NP_001165780.1:p.Gly377LeufsTer5
NM_144573.4:c.1321_1322del MANE Select	NP_653174.3:p.Gly441LeufsTer5