Canonical Allele Identifier: CA2567960201

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933583_77933585del , CM000663.2:g.77933583_77933585del	GRCh38
NC_000001.10:g.78399268_78399270del , CM000663.1:g.78399268_78399270del	GRCh37
NC_000001.9:g.78171856_78171858del	NCBI36
NG_016625.1:g.50069_50071del , LRG_442:g.50069_50071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+104_1251+106del MANE Select	ENSP00000333938.7:n.1251+104_1251+106del
ENST00000330010.12:c.1059+104_1059+106del	ENSP00000327363.8:n.1059+104_1059+106del
ENST00000334785.11:c.1251+104_1251+106del	ENSP00000333938.7:n.1251+104_1251+106del
ENST00000342754.5:c.950+104_950+106del
ENST00000440324.5:c.1209+104_1209+106del	ENSP00000411902.1:n.1209+104_1209+106del
ENST00000464998.1:n.711+104_711+106del
ENST00000480732.2:n.825+104_825+106del
NM_001172309.1:c.1059+104_1059+106del	NP_001165780.1:n.1059+104_1059+106del
NM_144573.3:c.1251+104_1251+106del , LRG_442t1:c.1251+104_1251+106del	NP_653174.3:n.1251+104_1251+106del
XM_005271322.2:c.1251+104_1251+106del	XP_005271379.1:n.1251+104_1251+106del
XM_005271323.2:c.1209+104_1209+106del	XP_005271380.1:n.1209+104_1209+106del
XM_005271324.3:c.1059+104_1059+106del	XP_005271381.1:n.1059+104_1059+106del
XM_005271325.2:c.1251+104_1251+106del	XP_005271382.1:n.1251+104_1251+106del
XM_005271326.2:c.1017+104_1017+106del	XP_005271383.1:n.1017+104_1017+106del
XM_005271327.2:c.834+104_834+106del	XP_005271384.1:n.834+104_834+106del
XM_005271322.4:c.1251+104_1251+106del	XP_005271379.1:n.1251+104_1251+106del
XM_005271323.4:c.1209+104_1209+106del	XP_005271380.1:n.1209+104_1209+106del
XM_005271324.5:c.1059+104_1059+106del	XP_005271381.1:n.1059+104_1059+106del
XM_005271325.4:c.1251+104_1251+106del	XP_005271382.1:n.1251+104_1251+106del
XM_005271326.4:c.1017+104_1017+106del	XP_005271383.1:n.1017+104_1017+106del
XM_005271327.4:c.834+104_834+106del	XP_005271384.1:n.834+104_834+106del
NM_001172309.2:c.1059+104_1059+106del	NP_001165780.1:n.1059+104_1059+106del
NM_144573.4:c.1251+104_1251+106del MANE Select	NP_653174.3:n.1251+104_1251+106del