Canonical Allele Identifier: CA340880571

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942027-A-G
• MyVariant Identifiers: chr1:g.78407712A>G (hg19) ; chr1:g.77942027A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942027A>G , CM000663.2:g.77942027A>G	GRCh38
NC_000001.10:g.78407712A>G , CM000663.1:g.78407712A>G	GRCh37
NC_000001.9:g.78180300A>G	NCBI36
NG_016625.1:g.58513A>G , LRG_442:g.58513A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1478A>G MANE Select	ENSP00000333938.7:p.Asp493Gly
ENST00000330010.12:c.1286A>G	ENSP00000327363.8:p.Asp429Gly
ENST00000334785.11:c.1478A>G	ENSP00000333938.7:p.Asp493Gly
ENST00000342754.5:c.1177A>G
ENST00000470735.1:n.317A>G
ENST00000480732.2:n.1052A>G
NM_001172309.1:c.1286A>G	NP_001165780.1:p.Asp429Gly
NM_144573.3:c.1478A>G , LRG_442t1:c.1478A>G	NP_653174.3:p.Asp493Gly
XM_005271322.2:c.1478A>G	XP_005271379.1:p.Asp493Gly
XM_005271323.2:c.1436A>G	XP_005271380.1:p.Asp479Gly
XM_005271324.3:c.1286A>G	XP_005271381.1:p.Asp429Gly
XM_005271325.2:c.1256A>G	XP_005271382.1:p.Asp419Gly
XM_005271326.2:c.1244A>G	XP_005271383.1:p.Asp415Gly
XM_005271327.2:c.1061A>G	XP_005271384.1:p.Asp354Gly
XM_005271322.4:c.1478A>G	XP_005271379.1:p.Asp493Gly
XM_005271323.4:c.1436A>G	XP_005271380.1:p.Asp479Gly
XM_005271324.5:c.1286A>G	XP_005271381.1:p.Asp429Gly
XM_005271325.4:c.1256A>G	XP_005271382.1:p.Asp419Gly
XM_005271326.4:c.1244A>G	XP_005271383.1:p.Asp415Gly
XM_005271327.4:c.1061A>G	XP_005271384.1:p.Asp354Gly
NM_001172309.2:c.1286A>G	NP_001165780.1:p.Asp429Gly
NM_144573.4:c.1478A>G MANE Select	NP_653174.3:p.Asp493Gly