Canonical Allele Identifier: CA1177628125

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935527_77935528delinsGC , CM000663.2:g.77935527_77935528delinsGC	GRCh38
NC_000001.10:g.78401212_78401213delinsGC , CM000663.1:g.78401212_78401213delinsGC	GRCh37
NC_000001.9:g.78173800_78173801delinsGC	NCBI36
NG_016625.1:g.52013_52014delinsGC , LRG_442:g.52013_52014delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-296_1252-295delinsGC MANE Select	ENSP00000333938.7:n.1252-296_1252-295delinsGC
ENST00000330010.12:c.1060-296_1060-295delinsGC	ENSP00000327363.8:n.1060-296_1060-295delinsGC
ENST00000334785.11:c.1252-296_1252-295delinsGC	ENSP00000333938.7:n.1252-296_1252-295delinsGC
ENST00000342754.5:c.951-296_951-295delinsGC
ENST00000440324.5:c.1210-296_1210-295delinsGC	ENSP00000411902.1:n.1210-296_1210-295delinsGC
ENST00000464998.1:n.712-296_712-295delinsGC
ENST00000480732.2:n.826-296_826-295delinsGC
NM_001172309.1:c.1060-296_1060-295delinsGC	NP_001165780.1:n.1060-296_1060-295delinsGC
NM_144573.3:c.1252-296_1252-295delinsGC , LRG_442t1:c.1252-296_1252-295delinsGC	NP_653174.3:n.1252-296_1252-295delinsGC
XM_005271322.2:c.1252-296_1252-295delinsGC	XP_005271379.1:n.1252-296_1252-295delinsGC
XM_005271323.2:c.1210-296_1210-295delinsGC	XP_005271380.1:n.1210-296_1210-295delinsGC
XM_005271324.3:c.1060-296_1060-295delinsGC	XP_005271381.1:n.1060-296_1060-295delinsGC
XM_005271325.2:c.1251+2048_1251+2049delinsGC	XP_005271382.1:n.1251+2048_1251+2049delinsGC
XM_005271326.2:c.1018-296_1018-295delinsGC	XP_005271383.1:n.1018-296_1018-295delinsGC
XM_005271327.2:c.835-296_835-295delinsGC	XP_005271384.1:n.835-296_835-295delinsGC
XM_005271322.4:c.1252-296_1252-295delinsGC	XP_005271379.1:n.1252-296_1252-295delinsGC
XM_005271323.4:c.1210-296_1210-295delinsGC	XP_005271380.1:n.1210-296_1210-295delinsGC
XM_005271324.5:c.1060-296_1060-295delinsGC	XP_005271381.1:n.1060-296_1060-295delinsGC
XM_005271325.4:c.1251+2048_1251+2049delinsGC	XP_005271382.1:n.1251+2048_1251+2049delinsGC
XM_005271326.4:c.1018-296_1018-295delinsGC	XP_005271383.1:n.1018-296_1018-295delinsGC
XM_005271327.4:c.835-296_835-295delinsGC	XP_005271384.1:n.835-296_835-295delinsGC
NM_001172309.2:c.1060-296_1060-295delinsGC	NP_001165780.1:n.1060-296_1060-295delinsGC
NM_144573.4:c.1252-296_1252-295delinsGC MANE Select	NP_653174.3:n.1252-296_1252-295delinsGC