Canonical Allele Identifier: CA2646274712

Gene: NEXN

Linked Data

• gnomAD v4: 1-77935837-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935838del , CM000663.2:g.77935838del	GRCh38
NC_000001.10:g.78401523del , CM000663.1:g.78401523del	GRCh37
NC_000001.9:g.78174111del	NCBI36
NG_016625.1:g.52324del , LRG_442:g.52324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1267del MANE Select	ENSP00000333938.7:p.Glu423LysfsTer5
ENST00000330010.12:c.1075del	ENSP00000327363.8:p.Glu359LysfsTer5
ENST00000334785.11:c.1267del	ENSP00000333938.7:p.Glu423LysfsTer5
ENST00000342754.5:c.966del
ENST00000440324.5:c.1225del	ENSP00000411902.1:p.Glu409LysfsTer5
ENST00000464998.1:n.727del
ENST00000480732.2:n.841del
NM_001172309.1:c.1075del	NP_001165780.1:p.Glu359LysfsTer5
NM_144573.3:c.1267del , LRG_442t1:c.1267del	NP_653174.3:p.Glu423LysfsTer5
XM_005271322.2:c.1267del	XP_005271379.1:p.Glu423LysfsTer5
XM_005271323.2:c.1225del	XP_005271380.1:p.Glu409LysfsTer5
XM_005271324.3:c.1075del	XP_005271381.1:p.Glu359LysfsTer5
XM_005271325.2:c.1251+2359del	XP_005271382.1:n.1251+2359del
XM_005271326.2:c.1033del	XP_005271383.1:p.Glu345LysfsTer5
XM_005271327.2:c.850del	XP_005271384.1:p.Glu284LysfsTer5
XM_005271322.4:c.1267del	XP_005271379.1:p.Glu423LysfsTer5
XM_005271323.4:c.1225del	XP_005271380.1:p.Glu409LysfsTer5
XM_005271324.5:c.1075del	XP_005271381.1:p.Glu359LysfsTer5
XM_005271325.4:c.1251+2359del	XP_005271382.1:n.1251+2359del
XM_005271326.4:c.1033del	XP_005271383.1:p.Glu345LysfsTer5
XM_005271327.4:c.850del	XP_005271384.1:p.Glu284LysfsTer5
NM_001172309.2:c.1075del	NP_001165780.1:p.Glu359LysfsTer5
NM_144573.4:c.1267del MANE Select	NP_653174.3:p.Glu423LysfsTer5