Canonical Allele Identifier: CA524231078

Gene: NEXN

Linked Data

• gnomAD v2: 1-78407841-A-AT
• MyVariant Identifiers: chr1:g.78407841_78407842insT (hg19) ; chr1:g.77942156_77942157insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942156_77942157insT , CM000663.2:g.77942156_77942157insT	GRCh38
NC_000001.10:g.78407841_78407842insT , CM000663.1:g.78407841_78407842insT	GRCh37
NC_000001.9:g.78180429_78180430insT	NCBI36
NG_016625.1:g.58642_58643insT , LRG_442:g.58642_58643insT
NG_033243.2:g.41937_41938insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1607_1608insT MANE Select	ENSP00000333938.7:p.Lys536AsnfsTer8
ENST00000330010.12:c.1415_1416insT	ENSP00000327363.8:p.Lys472AsnfsTer8
ENST00000334785.11:c.1607_1608insT	ENSP00000333938.7:p.Lys536AsnfsTer8
ENST00000342754.5:c.1306_1307insT
ENST00000470735.1:n.446_447insT
ENST00000480732.2:n.1181_1182insT
NM_001172309.1:c.1415_1416insT	NP_001165780.1:p.Lys472AsnfsTer8
NM_144573.3:c.1607_1608insT , LRG_442t1:c.1607_1608insT	NP_653174.3:p.Lys536AsnfsTer8
XM_005271322.2:c.1607_1608insT	XP_005271379.1:p.Lys536AsnfsTer8
XM_005271323.2:c.1565_1566insT	XP_005271380.1:p.Lys522AsnfsTer8
XM_005271324.3:c.1415_1416insT	XP_005271381.1:p.Lys472AsnfsTer8
XM_005271325.2:c.1385_1386insT	XP_005271382.1:p.Lys462AsnfsTer8
XM_005271326.2:c.1373_1374insT	XP_005271383.1:p.Lys458AsnfsTer8
XM_005271327.2:c.1190_1191insT	XP_005271384.1:p.Lys397AsnfsTer8
XM_005271322.4:c.1607_1608insT	XP_005271379.1:p.Lys536AsnfsTer8
XM_005271323.4:c.1565_1566insT	XP_005271380.1:p.Lys522AsnfsTer8
XM_005271324.5:c.1415_1416insT	XP_005271381.1:p.Lys472AsnfsTer8
XM_005271325.4:c.1385_1386insT	XP_005271382.1:p.Lys462AsnfsTer8
XM_005271326.4:c.1373_1374insT	XP_005271383.1:p.Lys458AsnfsTer8
XM_005271327.4:c.1190_1191insT	XP_005271384.1:p.Lys397AsnfsTer8
NM_001172309.2:c.1415_1416insT	NP_001165780.1:p.Lys472AsnfsTer8
NM_144573.4:c.1607_1608insT MANE Select	NP_653174.3:p.Lys536AsnfsTer8