Canonical Allele Identifier: CA1177628324

Gene: NEXN

Linked Data

• dbSNP Id: rs397517846

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935978_77935980dup , CM000663.2:g.77935978_77935980dup	GRCh38
NC_000001.10:g.78401663_78401665dup , CM000663.1:g.78401663_78401665dup	GRCh37
NC_000001.9:g.78174251_78174253dup	NCBI36
NG_016625.1:g.52464_52466dup , LRG_442:g.52464_52466dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1407_1409dup MANE Select	ENSP00000333938.7:p.Glu470_Arg471insGlu
ENST00000330010.12:c.1215_1217dup	ENSP00000327363.8:p.Glu406_Arg407insGlu
ENST00000334785.11:c.1407_1409dup	ENSP00000333938.7:p.Glu470_Arg471insGlu
ENST00000342754.5:c.1106_1108dup
ENST00000480732.2:n.981_983dup
NM_001172309.1:c.1215_1217dup	NP_001165780.1:p.Glu406_Arg407insGlu
NM_144573.3:c.1407_1409dup , LRG_442t1:c.1407_1409dup	NP_653174.3:p.Glu470_Arg471insGlu
XM_005271322.2:c.1407_1409dup	XP_005271379.1:p.Glu470_Arg471insGlu
XM_005271323.2:c.1365_1367dup	XP_005271380.1:p.Glu456_Arg457insGlu
XM_005271324.3:c.1215_1217dup	XP_005271381.1:p.Glu406_Arg407insGlu
XM_005271325.2:c.1251+2499_1251+2501dup	XP_005271382.1:n.1251+2499_1251+2501dup
XM_005271326.2:c.1173_1175dup	XP_005271383.1:p.Glu392_Arg393insGlu
XM_005271327.2:c.990_992dup	XP_005271384.1:p.Glu331_Arg332insGlu
XM_005271322.4:c.1407_1409dup	XP_005271379.1:p.Glu470_Arg471insGlu
XM_005271323.4:c.1365_1367dup	XP_005271380.1:p.Glu456_Arg457insGlu
XM_005271324.5:c.1215_1217dup	XP_005271381.1:p.Glu406_Arg407insGlu
XM_005271325.4:c.1251+2499_1251+2501dup	XP_005271382.1:n.1251+2499_1251+2501dup
XM_005271326.4:c.1173_1175dup	XP_005271383.1:p.Glu392_Arg393insGlu
XM_005271327.4:c.990_992dup	XP_005271384.1:p.Glu331_Arg332insGlu
NM_001172309.2:c.1215_1217dup	NP_001165780.1:p.Glu406_Arg407insGlu
NM_144573.4:c.1407_1409dup MANE Select	NP_653174.3:p.Glu470_Arg471insGlu