Canonical Allele Identifier: CA2556457933

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933557_77933558insCTAA , CM000663.2:g.77933557_77933558insCTAA	GRCh38
NC_000001.10:g.78399242_78399243insCTAA , CM000663.1:g.78399242_78399243insCTAA	GRCh37
NC_000001.9:g.78171830_78171831insCTAA	NCBI36
NG_016625.1:g.50043_50044insCTAA , LRG_442:g.50043_50044insCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+78_1251+79insCTAA MANE Select	ENSP00000333938.7:n.1251+78_1251+79insCTAA
ENST00000330010.12:c.1059+78_1059+79insCTAA	ENSP00000327363.8:n.1059+78_1059+79insCTAA
ENST00000334785.11:c.1251+78_1251+79insCTAA	ENSP00000333938.7:n.1251+78_1251+79insCTAA
ENST00000342754.5:c.950+78_950+79insCTAA
ENST00000440324.5:c.1209+78_1209+79insCTAA	ENSP00000411902.1:n.1209+78_1209+79insCTAA
ENST00000464998.1:n.711+78_711+79insCTAA
ENST00000480732.2:n.825+78_825+79insCTAA
NM_001172309.1:c.1059+78_1059+79insCTAA	NP_001165780.1:n.1059+78_1059+79insCTAA
NM_144573.3:c.1251+78_1251+79insCTAA , LRG_442t1:c.1251+78_1251+79insCTAA	NP_653174.3:n.1251+78_1251+79insCTAA
XM_005271322.2:c.1251+78_1251+79insCTAA	XP_005271379.1:n.1251+78_1251+79insCTAA
XM_005271323.2:c.1209+78_1209+79insCTAA	XP_005271380.1:n.1209+78_1209+79insCTAA
XM_005271324.3:c.1059+78_1059+79insCTAA	XP_005271381.1:n.1059+78_1059+79insCTAA
XM_005271325.2:c.1251+78_1251+79insCTAA	XP_005271382.1:n.1251+78_1251+79insCTAA
XM_005271326.2:c.1017+78_1017+79insCTAA	XP_005271383.1:n.1017+78_1017+79insCTAA
XM_005271327.2:c.834+78_834+79insCTAA	XP_005271384.1:n.834+78_834+79insCTAA
XM_005271322.4:c.1251+78_1251+79insCTAA	XP_005271379.1:n.1251+78_1251+79insCTAA
XM_005271323.4:c.1209+78_1209+79insCTAA	XP_005271380.1:n.1209+78_1209+79insCTAA
XM_005271324.5:c.1059+78_1059+79insCTAA	XP_005271381.1:n.1059+78_1059+79insCTAA
XM_005271325.4:c.1251+78_1251+79insCTAA	XP_005271382.1:n.1251+78_1251+79insCTAA
XM_005271326.4:c.1017+78_1017+79insCTAA	XP_005271383.1:n.1017+78_1017+79insCTAA
XM_005271327.4:c.834+78_834+79insCTAA	XP_005271384.1:n.834+78_834+79insCTAA
NM_001172309.2:c.1059+78_1059+79insCTAA	NP_001165780.1:n.1059+78_1059+79insCTAA
NM_144573.4:c.1251+78_1251+79insCTAA MANE Select	NP_653174.3:n.1251+78_1251+79insCTAA