Canonical Allele Identifier: CA1177626909

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933596_77933597delinsAT , CM000663.2:g.77933596_77933597delinsAT	GRCh38
NC_000001.10:g.78399281_78399282delinsAT , CM000663.1:g.78399281_78399282delinsAT	GRCh37
NC_000001.9:g.78171869_78171870delinsAT	NCBI36
NG_016625.1:g.50082_50083delinsAT , LRG_442:g.50082_50083delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+117_1251+118delinsAT MANE Select	ENSP00000333938.7:n.1251+117_1251+118delinsAT
ENST00000330010.12:c.1059+117_1059+118delinsAT	ENSP00000327363.8:n.1059+117_1059+118delinsAT
ENST00000334785.11:c.1251+117_1251+118delinsAT	ENSP00000333938.7:n.1251+117_1251+118delinsAT
ENST00000342754.5:c.950+117_950+118delinsAT
ENST00000440324.5:c.1209+117_1209+118delinsAT	ENSP00000411902.1:n.1209+117_1209+118delinsAT
ENST00000464998.1:n.711+117_711+118delinsAT
ENST00000480732.2:n.825+117_825+118delinsAT
NM_001172309.1:c.1059+117_1059+118delinsAT	NP_001165780.1:n.1059+117_1059+118delinsAT
NM_144573.3:c.1251+117_1251+118delinsAT , LRG_442t1:c.1251+117_1251+118delinsAT	NP_653174.3:n.1251+117_1251+118delinsAT
XM_005271322.2:c.1251+117_1251+118delinsAT	XP_005271379.1:n.1251+117_1251+118delinsAT
XM_005271323.2:c.1209+117_1209+118delinsAT	XP_005271380.1:n.1209+117_1209+118delinsAT
XM_005271324.3:c.1059+117_1059+118delinsAT	XP_005271381.1:n.1059+117_1059+118delinsAT
XM_005271325.2:c.1251+117_1251+118delinsAT	XP_005271382.1:n.1251+117_1251+118delinsAT
XM_005271326.2:c.1017+117_1017+118delinsAT	XP_005271383.1:n.1017+117_1017+118delinsAT
XM_005271327.2:c.834+117_834+118delinsAT	XP_005271384.1:n.834+117_834+118delinsAT
XM_005271322.4:c.1251+117_1251+118delinsAT	XP_005271379.1:n.1251+117_1251+118delinsAT
XM_005271323.4:c.1209+117_1209+118delinsAT	XP_005271380.1:n.1209+117_1209+118delinsAT
XM_005271324.5:c.1059+117_1059+118delinsAT	XP_005271381.1:n.1059+117_1059+118delinsAT
XM_005271325.4:c.1251+117_1251+118delinsAT	XP_005271382.1:n.1251+117_1251+118delinsAT
XM_005271326.4:c.1017+117_1017+118delinsAT	XP_005271383.1:n.1017+117_1017+118delinsAT
XM_005271327.4:c.834+117_834+118delinsAT	XP_005271384.1:n.834+117_834+118delinsAT
NM_001172309.2:c.1059+117_1059+118delinsAT	NP_001165780.1:n.1059+117_1059+118delinsAT
NM_144573.4:c.1251+117_1251+118delinsAT MANE Select	NP_653174.3:n.1251+117_1251+118delinsAT