Canonical Allele Identifier: CA524231071

Gene: NEXN

Linked Data

• dbSNP Id: rs1215574212
• gnomAD v2: 1-78407798-A-AT
• gnomAD v4: 1-77942113-A-AT
• MyVariant Identifiers: chr1:g.78407798_78407799insT (hg19) ; chr1:g.77942113_77942114insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942113_77942114insT , CM000663.2:g.77942113_77942114insT	GRCh38
NC_000001.10:g.78407798_78407799insT , CM000663.1:g.78407798_78407799insT	GRCh37
NC_000001.9:g.78180386_78180387insT	NCBI36
NG_016625.1:g.58599_58600insT , LRG_442:g.58599_58600insT
NG_033243.2:g.41980_41981insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1564_1565insT MANE Select	ENSP00000333938.7:p.Lys522IlefsTer12
ENST00000330010.12:c.1372_1373insT	ENSP00000327363.8:p.Lys458IlefsTer12
ENST00000334785.11:c.1564_1565insT	ENSP00000333938.7:p.Lys522IlefsTer12
ENST00000342754.5:c.1263_1264insT
ENST00000470735.1:n.403_404insT
ENST00000480732.2:n.1138_1139insT
NM_001172309.1:c.1372_1373insT	NP_001165780.1:p.Lys458IlefsTer12
NM_144573.3:c.1564_1565insT , LRG_442t1:c.1564_1565insT	NP_653174.3:p.Lys522IlefsTer12
XM_005271322.2:c.1564_1565insT	XP_005271379.1:p.Lys522IlefsTer12
XM_005271323.2:c.1522_1523insT	XP_005271380.1:p.Lys508IlefsTer12
XM_005271324.3:c.1372_1373insT	XP_005271381.1:p.Lys458IlefsTer12
XM_005271325.2:c.1342_1343insT	XP_005271382.1:p.Lys448IlefsTer12
XM_005271326.2:c.1330_1331insT	XP_005271383.1:p.Lys444IlefsTer12
XM_005271327.2:c.1147_1148insT	XP_005271384.1:p.Lys383IlefsTer12
XM_005271322.4:c.1564_1565insT	XP_005271379.1:p.Lys522IlefsTer12
XM_005271323.4:c.1522_1523insT	XP_005271380.1:p.Lys508IlefsTer12
XM_005271324.5:c.1372_1373insT	XP_005271381.1:p.Lys458IlefsTer12
XM_005271325.4:c.1342_1343insT	XP_005271382.1:p.Lys448IlefsTer12
XM_005271326.4:c.1330_1331insT	XP_005271383.1:p.Lys444IlefsTer12
XM_005271327.4:c.1147_1148insT	XP_005271384.1:p.Lys383IlefsTer12
NM_001172309.2:c.1372_1373insT	NP_001165780.1:p.Lys458IlefsTer12
NM_144573.4:c.1564_1565insT MANE Select	NP_653174.3:p.Lys522IlefsTer12