Canonical Allele Identifier: CA1177628322

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935971_77935974delinsTAGA , CM000663.2:g.77935971_77935974delinsTAGA	GRCh38
NC_000001.10:g.78401656_78401659delinsTAGA , CM000663.1:g.78401656_78401659delinsTAGA	GRCh37
NC_000001.9:g.78174244_78174247delinsTAGA	NCBI36
NG_016625.1:g.52457_52460delinsTAGA , LRG_442:g.52457_52460delinsTAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1400_1403delinsTAGA MANE Select	ENSP00000333938.7:p.Ile467=
ENST00000330010.12:c.1208_1211delinsTAGA	ENSP00000327363.8:p.Ile403=
ENST00000334785.11:c.1400_1403delinsTAGA	ENSP00000333938.7:p.Ile467=
ENST00000342754.5:c.1099_1102delinsTAGA
ENST00000480732.2:n.974_977delinsTAGA
NM_001172309.1:c.1208_1211delinsTAGA	NP_001165780.1:p.Ile403=
NM_144573.3:c.1400_1403delinsTAGA , LRG_442t1:c.1400_1403delinsTAGA	NP_653174.3:p.Ile467=
XM_005271322.2:c.1400_1403delinsTAGA	XP_005271379.1:p.Ile467=
XM_005271323.2:c.1358_1361delinsTAGA	XP_005271380.1:p.Ile453=
XM_005271324.3:c.1208_1211delinsTAGA	XP_005271381.1:p.Ile403=
XM_005271325.2:c.1251+2492_1251+2495delinsTAGA	XP_005271382.1:n.1251+2492_1251+2495delinsTAGA
XM_005271326.2:c.1166_1169delinsTAGA	XP_005271383.1:p.Ile389=
XM_005271327.2:c.983_986delinsTAGA	XP_005271384.1:p.Ile328=
XM_005271322.4:c.1400_1403delinsTAGA	XP_005271379.1:p.Ile467=
XM_005271323.4:c.1358_1361delinsTAGA	XP_005271380.1:p.Ile453=
XM_005271324.5:c.1208_1211delinsTAGA	XP_005271381.1:p.Ile403=
XM_005271325.4:c.1251+2492_1251+2495delinsTAGA	XP_005271382.1:n.1251+2492_1251+2495delinsTAGA
XM_005271326.4:c.1166_1169delinsTAGA	XP_005271383.1:p.Ile389=
XM_005271327.4:c.983_986delinsTAGA	XP_005271384.1:p.Ile328=
NM_001172309.2:c.1208_1211delinsTAGA	NP_001165780.1:p.Ile403=
NM_144573.4:c.1400_1403delinsTAGA MANE Select	NP_653174.3:p.Ile467=