Canonical Allele Identifier: CA1177628323

Gene: NEXN

Linked Data

• dbSNP Id: rs1650725065

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935971_77935973del , CM000663.2:g.77935971_77935973del	GRCh38
NC_000001.10:g.78401656_78401658del , CM000663.1:g.78401656_78401658del	GRCh37
NC_000001.9:g.78174244_78174246del	NCBI36
NG_016625.1:g.52457_52459del , LRG_442:g.52457_52459del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1400_1402del MANE Select	ENSP00000333938.7:p.Ile467_Glu468delinsLys
ENST00000330010.12:c.1208_1210del	ENSP00000327363.8:p.Ile403_Glu404delinsLys
ENST00000334785.11:c.1400_1402del	ENSP00000333938.7:p.Ile467_Glu468delinsLys
ENST00000342754.5:c.1099_1101del
ENST00000480732.2:n.974_976del
NM_001172309.1:c.1208_1210del	NP_001165780.1:p.Ile403_Glu404delinsLys
NM_144573.3:c.1400_1402del , LRG_442t1:c.1400_1402del	NP_653174.3:p.Ile467_Glu468delinsLys
XM_005271322.2:c.1400_1402del	XP_005271379.1:p.Ile467_Glu468delinsLys
XM_005271323.2:c.1358_1360del	XP_005271380.1:p.Ile453_Glu454delinsLys
XM_005271324.3:c.1208_1210del	XP_005271381.1:p.Ile403_Glu404delinsLys
XM_005271325.2:c.1251+2492_1251+2494del	XP_005271382.1:n.1251+2492_1251+2494del
XM_005271326.2:c.1166_1168del	XP_005271383.1:p.Ile389_Glu390delinsLys
XM_005271327.2:c.983_985del	XP_005271384.1:p.Ile328_Glu329delinsLys
XM_005271322.4:c.1400_1402del	XP_005271379.1:p.Ile467_Glu468delinsLys
XM_005271323.4:c.1358_1360del	XP_005271380.1:p.Ile453_Glu454delinsLys
XM_005271324.5:c.1208_1210del	XP_005271381.1:p.Ile403_Glu404delinsLys
XM_005271325.4:c.1251+2492_1251+2494del	XP_005271382.1:n.1251+2492_1251+2494del
XM_005271326.4:c.1166_1168del	XP_005271383.1:p.Ile389_Glu390delinsLys
XM_005271327.4:c.983_985del	XP_005271384.1:p.Ile328_Glu329delinsLys
NM_001172309.2:c.1208_1210del	NP_001165780.1:p.Ile403_Glu404delinsLys
NM_144573.4:c.1400_1402del MANE Select	NP_653174.3:p.Ile467_Glu468delinsLys