Canonical Allele Identifier: CA340880573

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942028-T-A
• MyVariant Identifiers: chr1:g.78407713T>A (hg19) ; chr1:g.77942028T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942028T>A , CM000663.2:g.77942028T>A	GRCh38
NC_000001.10:g.78407713T>A , CM000663.1:g.78407713T>A	GRCh37
NC_000001.9:g.78180301T>A	NCBI36
NG_016625.1:g.58514T>A , LRG_442:g.58514T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1479T>A MANE Select	ENSP00000333938.7:p.Asp493Glu
ENST00000330010.12:c.1287T>A	ENSP00000327363.8:p.Asp429Glu
ENST00000334785.11:c.1479T>A	ENSP00000333938.7:p.Asp493Glu
ENST00000342754.5:c.1178T>A
ENST00000470735.1:n.318T>A
ENST00000480732.2:n.1053T>A
NM_001172309.1:c.1287T>A	NP_001165780.1:p.Asp429Glu
NM_144573.3:c.1479T>A , LRG_442t1:c.1479T>A	NP_653174.3:p.Asp493Glu
XM_005271322.2:c.1479T>A	XP_005271379.1:p.Asp493Glu
XM_005271323.2:c.1437T>A	XP_005271380.1:p.Asp479Glu
XM_005271324.3:c.1287T>A	XP_005271381.1:p.Asp429Glu
XM_005271325.2:c.1257T>A	XP_005271382.1:p.Asp419Glu
XM_005271326.2:c.1245T>A	XP_005271383.1:p.Asp415Glu
XM_005271327.2:c.1062T>A	XP_005271384.1:p.Asp354Glu
XM_005271322.4:c.1479T>A	XP_005271379.1:p.Asp493Glu
XM_005271323.4:c.1437T>A	XP_005271380.1:p.Asp479Glu
XM_005271324.5:c.1287T>A	XP_005271381.1:p.Asp429Glu
XM_005271325.4:c.1257T>A	XP_005271382.1:p.Asp419Glu
XM_005271326.4:c.1245T>A	XP_005271383.1:p.Asp415Glu
XM_005271327.4:c.1062T>A	XP_005271384.1:p.Asp354Glu
NM_001172309.2:c.1287T>A	NP_001165780.1:p.Asp429Glu
NM_144573.4:c.1479T>A MANE Select	NP_653174.3:p.Asp493Glu