Canonical Allele Identifier: CA1177631211

Gene: NEXN

Linked Data

• dbSNP Id: rs1651394597

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942207del , CM000663.2:g.77942207del	GRCh38
NC_000001.10:g.78407892del , CM000663.1:g.78407892del	GRCh37
NC_000001.9:g.78180480del	NCBI36
NG_016625.1:g.58693del , LRG_442:g.58693del
NG_033243.2:g.41890del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1658del MANE Select	ENSP00000333938.7:p.Lys553ArgfsTer14
ENST00000330010.12:c.1466del	ENSP00000327363.8:p.Lys489ArgfsTer14
ENST00000334785.11:c.1658del	ENSP00000333938.7:p.Lys553ArgfsTer14
ENST00000342754.5:c.1357del
ENST00000470735.1:n.497del
ENST00000480732.2:n.1232del
NM_001172309.1:c.1466del	NP_001165780.1:p.Lys489ArgfsTer14
NM_144573.3:c.1658del , LRG_442t1:c.1658del	NP_653174.3:p.Lys553ArgfsTer14
XM_005271322.2:c.1658del	XP_005271379.1:p.Lys553ArgfsTer14
XM_005271323.2:c.1616del	XP_005271380.1:p.Lys539ArgfsTer14
XM_005271324.3:c.1466del	XP_005271381.1:p.Lys489ArgfsTer14
XM_005271325.2:c.1436del	XP_005271382.1:p.Lys479ArgfsTer14
XM_005271326.2:c.1424del	XP_005271383.1:p.Lys475ArgfsTer14
XM_005271327.2:c.1241del	XP_005271384.1:p.Lys414ArgfsTer14
XM_005271322.4:c.1658del	XP_005271379.1:p.Lys553ArgfsTer14
XM_005271323.4:c.1616del	XP_005271380.1:p.Lys539ArgfsTer14
XM_005271324.5:c.1466del	XP_005271381.1:p.Lys489ArgfsTer14
XM_005271325.4:c.1436del	XP_005271382.1:p.Lys479ArgfsTer14
XM_005271326.4:c.1424del	XP_005271383.1:p.Lys475ArgfsTer14
XM_005271327.4:c.1241del	XP_005271384.1:p.Lys414ArgfsTer14
NM_001172309.2:c.1466del	NP_001165780.1:p.Lys489ArgfsTer14
NM_144573.4:c.1658del MANE Select	NP_653174.3:p.Lys553ArgfsTer14