Canonical Allele Identifier: CA2646274781

Gene: NEXN

Linked Data

• gnomAD v4: 1-77936193-A-AGATC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936194_77936197dup , CM000663.2:g.77936194_77936197dup	GRCh38
NC_000001.10:g.78401879_78401882dup , CM000663.1:g.78401879_78401882dup	GRCh37
NC_000001.9:g.78174467_78174470dup	NCBI36
NG_016625.1:g.52680_52683dup , LRG_442:g.52680_52683dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+150_1473+153dup MANE Select	ENSP00000333938.7:n.1473+150_1473+153dup
ENST00000330010.12:c.1281+150_1281+153dup	ENSP00000327363.8:n.1281+150_1281+153dup
ENST00000334785.11:c.1473+150_1473+153dup	ENSP00000333938.7:n.1473+150_1473+153dup
ENST00000342754.5:c.1172+150_1172+153dup
ENST00000480732.2:n.1047+150_1047+153dup
NM_001172309.1:c.1281+150_1281+153dup	NP_001165780.1:n.1281+150_1281+153dup
NM_144573.3:c.1473+150_1473+153dup , LRG_442t1:c.1473+150_1473+153dup	NP_653174.3:n.1473+150_1473+153dup
XM_005271322.2:c.1473+150_1473+153dup	XP_005271379.1:n.1473+150_1473+153dup
XM_005271323.2:c.1431+150_1431+153dup	XP_005271380.1:n.1431+150_1431+153dup
XM_005271324.3:c.1281+150_1281+153dup	XP_005271381.1:n.1281+150_1281+153dup
XM_005271325.2:c.1251+2715_1251+2718dup	XP_005271382.1:n.1251+2715_1251+2718dup
XM_005271326.2:c.1239+150_1239+153dup	XP_005271383.1:n.1239+150_1239+153dup
XM_005271327.2:c.1056+150_1056+153dup	XP_005271384.1:n.1056+150_1056+153dup
XM_005271322.4:c.1473+150_1473+153dup	XP_005271379.1:n.1473+150_1473+153dup
XM_005271323.4:c.1431+150_1431+153dup	XP_005271380.1:n.1431+150_1431+153dup
XM_005271324.5:c.1281+150_1281+153dup	XP_005271381.1:n.1281+150_1281+153dup
XM_005271325.4:c.1251+2715_1251+2718dup	XP_005271382.1:n.1251+2715_1251+2718dup
XM_005271326.4:c.1239+150_1239+153dup	XP_005271383.1:n.1239+150_1239+153dup
XM_005271327.4:c.1056+150_1056+153dup	XP_005271384.1:n.1056+150_1056+153dup
NM_001172309.2:c.1281+150_1281+153dup	NP_001165780.1:n.1281+150_1281+153dup
NM_144573.4:c.1473+150_1473+153dup MANE Select	NP_653174.3:n.1473+150_1473+153dup