Canonical Allele Identifier: CA1003482936

Gene: NEXN

Linked Data

• dbSNP Id: rs1650721899
• gnomAD v3: 1-77935939-A-AC
• gnomAD v4: 1-77935939-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935940dup , CM000663.2:g.77935940dup	GRCh38
NC_000001.10:g.78401625dup , CM000663.1:g.78401625dup	GRCh37
NC_000001.9:g.78174213dup	NCBI36
NG_016625.1:g.52426dup , LRG_442:g.52426dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1369dup MANE Select	ENSP00000333938.7:p.Gln457ProfsTer4
ENST00000330010.12:c.1177dup	ENSP00000327363.8:p.Gln393ProfsTer4
ENST00000334785.11:c.1369dup	ENSP00000333938.7:p.Gln457ProfsTer4
ENST00000342754.5:c.1068dup
ENST00000464998.1:n.829dup
ENST00000480732.2:n.943dup
NM_001172309.1:c.1177dup	NP_001165780.1:p.Gln393ProfsTer4
NM_144573.3:c.1369dup , LRG_442t1:c.1369dup	NP_653174.3:p.Gln457ProfsTer4
XM_005271322.2:c.1369dup	XP_005271379.1:p.Gln457ProfsTer4
XM_005271323.2:c.1327dup	XP_005271380.1:p.Gln443ProfsTer4
XM_005271324.3:c.1177dup	XP_005271381.1:p.Gln393ProfsTer4
XM_005271325.2:c.1251+2461dup	XP_005271382.1:n.1251+2461dup
XM_005271326.2:c.1135dup	XP_005271383.1:p.Gln379ProfsTer4
XM_005271327.2:c.952dup	XP_005271384.1:p.Gln318ProfsTer4
XM_005271322.4:c.1369dup	XP_005271379.1:p.Gln457ProfsTer4
XM_005271323.4:c.1327dup	XP_005271380.1:p.Gln443ProfsTer4
XM_005271324.5:c.1177dup	XP_005271381.1:p.Gln393ProfsTer4
XM_005271325.4:c.1251+2461dup	XP_005271382.1:n.1251+2461dup
XM_005271326.4:c.1135dup	XP_005271383.1:p.Gln379ProfsTer4
XM_005271327.4:c.952dup	XP_005271384.1:p.Gln318ProfsTer4
NM_001172309.2:c.1177dup	NP_001165780.1:p.Gln393ProfsTer4
NM_144573.4:c.1369dup MANE Select	NP_653174.3:p.Gln457ProfsTer4