Canonical Allele Identifier: CA1177626880

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933558_77933561delinsGTAT , CM000663.2:g.77933558_77933561delinsGTAT	GRCh38
NC_000001.10:g.78399243_78399246delinsGTAT , CM000663.1:g.78399243_78399246delinsGTAT	GRCh37
NC_000001.9:g.78171831_78171834delinsGTAT	NCBI36
NG_016625.1:g.50044_50047delinsGTAT , LRG_442:g.50044_50047delinsGTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+79_1251+82delinsGTAT MANE Select	ENSP00000333938.7:n.1251+79_1251+82delinsGTAT
ENST00000330010.12:c.1059+79_1059+82delinsGTAT	ENSP00000327363.8:n.1059+79_1059+82delinsGTAT
ENST00000334785.11:c.1251+79_1251+82delinsGTAT	ENSP00000333938.7:n.1251+79_1251+82delinsGTAT
ENST00000342754.5:c.950+79_950+82delinsGTAT
ENST00000440324.5:c.1209+79_1209+82delinsGTAT	ENSP00000411902.1:n.1209+79_1209+82delinsGTAT
ENST00000464998.1:n.711+79_711+82delinsGTAT
ENST00000480732.2:n.825+79_825+82delinsGTAT
NM_001172309.1:c.1059+79_1059+82delinsGTAT	NP_001165780.1:n.1059+79_1059+82delinsGTAT
NM_144573.3:c.1251+79_1251+82delinsGTAT , LRG_442t1:c.1251+79_1251+82delinsGTAT	NP_653174.3:n.1251+79_1251+82delinsGTAT
XM_005271322.2:c.1251+79_1251+82delinsGTAT	XP_005271379.1:n.1251+79_1251+82delinsGTAT
XM_005271323.2:c.1209+79_1209+82delinsGTAT	XP_005271380.1:n.1209+79_1209+82delinsGTAT
XM_005271324.3:c.1059+79_1059+82delinsGTAT	XP_005271381.1:n.1059+79_1059+82delinsGTAT
XM_005271325.2:c.1251+79_1251+82delinsGTAT	XP_005271382.1:n.1251+79_1251+82delinsGTAT
XM_005271326.2:c.1017+79_1017+82delinsGTAT	XP_005271383.1:n.1017+79_1017+82delinsGTAT
XM_005271327.2:c.834+79_834+82delinsGTAT	XP_005271384.1:n.834+79_834+82delinsGTAT
XM_005271322.4:c.1251+79_1251+82delinsGTAT	XP_005271379.1:n.1251+79_1251+82delinsGTAT
XM_005271323.4:c.1209+79_1209+82delinsGTAT	XP_005271380.1:n.1209+79_1209+82delinsGTAT
XM_005271324.5:c.1059+79_1059+82delinsGTAT	XP_005271381.1:n.1059+79_1059+82delinsGTAT
XM_005271325.4:c.1251+79_1251+82delinsGTAT	XP_005271382.1:n.1251+79_1251+82delinsGTAT
XM_005271326.4:c.1017+79_1017+82delinsGTAT	XP_005271383.1:n.1017+79_1017+82delinsGTAT
XM_005271327.4:c.834+79_834+82delinsGTAT	XP_005271384.1:n.834+79_834+82delinsGTAT
NM_001172309.2:c.1059+79_1059+82delinsGTAT	NP_001165780.1:n.1059+79_1059+82delinsGTAT
NM_144573.4:c.1251+79_1251+82delinsGTAT MANE Select	NP_653174.3:n.1251+79_1251+82delinsGTAT