Canonical Allele Identifier: CA916213686

Gene: NEXN

Linked Data

• dbSNP Id: rs1571172316

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942142_77942151del , CM000663.2:g.77942142_77942151del	GRCh38
NC_000001.10:g.78407827_78407836del , CM000663.1:g.78407827_78407836del	GRCh37
NC_000001.9:g.78180415_78180424del	NCBI36
NG_016625.1:g.58628_58637del , LRG_442:g.58628_58637del
NG_033243.2:g.41943_41952del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1593_1602del MANE Select	ENSP00000333938.7:p.Arg531SerfsTer?
ENST00000330010.12:c.1401_1410del	ENSP00000327363.8:p.Arg467SerfsTer?
ENST00000334785.11:c.1593_1602del	ENSP00000333938.7:p.Arg531SerfsTer?
ENST00000342754.5:c.1292_1301del
ENST00000470735.1:n.432_441del
ENST00000480732.2:n.1167_1176del
NM_001172309.1:c.1401_1410del	NP_001165780.1:p.Arg467SerfsTer?
NM_144573.3:c.1593_1602del , LRG_442t1:c.1593_1602del	NP_653174.3:p.Arg531SerfsTer?
XM_005271322.2:c.1593_1602del	XP_005271379.1:p.Arg531SerfsTer?
XM_005271323.2:c.1551_1560del	XP_005271380.1:p.Arg517SerfsTer?
XM_005271324.3:c.1401_1410del	XP_005271381.1:p.Arg467SerfsTer?
XM_005271325.2:c.1371_1380del	XP_005271382.1:p.Arg457SerfsTer?
XM_005271326.2:c.1359_1368del	XP_005271383.1:p.Arg453SerfsTer?
XM_005271327.2:c.1176_1185del	XP_005271384.1:p.Arg392SerfsTer?
XM_005271322.4:c.1593_1602del	XP_005271379.1:p.Arg531SerfsTer?
XM_005271323.4:c.1551_1560del	XP_005271380.1:p.Arg517SerfsTer?
XM_005271324.5:c.1401_1410del	XP_005271381.1:p.Arg467SerfsTer?
XM_005271325.4:c.1371_1380del	XP_005271382.1:p.Arg457SerfsTer?
XM_005271326.4:c.1359_1368del	XP_005271383.1:p.Arg453SerfsTer?
XM_005271327.4:c.1176_1185del	XP_005271384.1:p.Arg392SerfsTer?
NM_001172309.2:c.1401_1410del	NP_001165780.1:p.Arg467SerfsTer?
NM_144573.4:c.1593_1602del MANE Select	NP_653174.3:p.Arg531SerfsTer?