Canonical Allele Identifier: CA1177628276

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935860_77935862delinsAAT , CM000663.2:g.77935860_77935862delinsAAT	GRCh38
NC_000001.10:g.78401545_78401547delinsAAT , CM000663.1:g.78401545_78401547delinsAAT	GRCh37
NC_000001.9:g.78174133_78174135delinsAAT	NCBI36
NG_016625.1:g.52346_52348delinsAAT , LRG_442:g.52346_52348delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1289_1291delinsAAT MANE Select	ENSP00000333938.7:p.Glu430=
ENST00000330010.12:c.1097_1099delinsAAT	ENSP00000327363.8:p.Glu366=
ENST00000334785.11:c.1289_1291delinsAAT	ENSP00000333938.7:p.Glu430=
ENST00000342754.5:c.988_990delinsAAT
ENST00000440324.5:c.1247_1249delinsAAT	ENSP00000411902.1:p.Glu416=
ENST00000464998.1:n.749_751delinsAAT
ENST00000480732.2:n.863_865delinsAAT
NM_001172309.1:c.1097_1099delinsAAT	NP_001165780.1:p.Glu366=
NM_144573.3:c.1289_1291delinsAAT , LRG_442t1:c.1289_1291delinsAAT	NP_653174.3:p.Glu430=
XM_005271322.2:c.1289_1291delinsAAT	XP_005271379.1:p.Glu430=
XM_005271323.2:c.1247_1249delinsAAT	XP_005271380.1:p.Glu416=
XM_005271324.3:c.1097_1099delinsAAT	XP_005271381.1:p.Glu366=
XM_005271325.2:c.1251+2381_1251+2383delinsAAT	XP_005271382.1:n.1251+2381_1251+2383delinsAAT
XM_005271326.2:c.1055_1057delinsAAT	XP_005271383.1:p.Glu352=
XM_005271327.2:c.872_874delinsAAT	XP_005271384.1:p.Glu291=
XM_005271322.4:c.1289_1291delinsAAT	XP_005271379.1:p.Glu430=
XM_005271323.4:c.1247_1249delinsAAT	XP_005271380.1:p.Glu416=
XM_005271324.5:c.1097_1099delinsAAT	XP_005271381.1:p.Glu366=
XM_005271325.4:c.1251+2381_1251+2383delinsAAT	XP_005271382.1:n.1251+2381_1251+2383delinsAAT
XM_005271326.4:c.1055_1057delinsAAT	XP_005271383.1:p.Glu352=
XM_005271327.4:c.872_874delinsAAT	XP_005271384.1:p.Glu291=
NM_001172309.2:c.1097_1099delinsAAT	NP_001165780.1:p.Glu366=
NM_144573.4:c.1289_1291delinsAAT MANE Select	NP_653174.3:p.Glu430=