Canonical Allele Identifier: CA2574414091

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933435_77933439dup , CM000663.2:g.77933435_77933439dup	GRCh38
NC_000001.10:g.78399120_78399124dup , CM000663.1:g.78399120_78399124dup	GRCh37
NC_000001.9:g.78171708_78171712dup	NCBI36
NG_016625.1:g.49921_49925dup , LRG_442:g.49921_49925dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1207_1211dup MANE Select	ENSP00000333938.7:p.Lys405TrpfsTer9
ENST00000330010.12:c.1015_1019dup	ENSP00000327363.8:p.Lys341TrpfsTer9
ENST00000334785.11:c.1207_1211dup	ENSP00000333938.7:p.Lys405TrpfsTer9
ENST00000342754.5:c.906_910dup
ENST00000440324.5:c.1165_1169dup	ENSP00000411902.1:p.Lys391TrpfsTer9
ENST00000464998.1:n.667_671dup
ENST00000480732.2:n.781_785dup
NM_001172309.1:c.1015_1019dup	NP_001165780.1:p.Lys341TrpfsTer9
NM_144573.3:c.1207_1211dup , LRG_442t1:c.1207_1211dup	NP_653174.3:p.Lys405TrpfsTer9
XM_005271322.2:c.1207_1211dup	XP_005271379.1:p.Lys405TrpfsTer9
XM_005271323.2:c.1165_1169dup	XP_005271380.1:p.Lys391TrpfsTer9
XM_005271324.3:c.1015_1019dup	XP_005271381.1:p.Lys341TrpfsTer9
XM_005271325.2:c.1207_1211dup	XP_005271382.1:p.Lys405TrpfsTer9
XM_005271326.2:c.973_977dup	XP_005271383.1:p.Lys327TrpfsTer9
XM_005271327.2:c.790_794dup	XP_005271384.1:p.Lys266TrpfsTer9
XM_005271322.4:c.1207_1211dup	XP_005271379.1:p.Lys405TrpfsTer9
XM_005271323.4:c.1165_1169dup	XP_005271380.1:p.Lys391TrpfsTer9
XM_005271324.5:c.1015_1019dup	XP_005271381.1:p.Lys341TrpfsTer9
XM_005271325.4:c.1207_1211dup	XP_005271382.1:p.Lys405TrpfsTer9
XM_005271326.4:c.973_977dup	XP_005271383.1:p.Lys327TrpfsTer9
XM_005271327.4:c.790_794dup	XP_005271384.1:p.Lys266TrpfsTer9
NM_001172309.2:c.1015_1019dup	NP_001165780.1:p.Lys341TrpfsTer9
NM_144573.4:c.1207_1211dup MANE Select	NP_653174.3:p.Lys405TrpfsTer9