Canonical Allele Identifier: CA340876722

Gene: NEXN

Linked Data

• gnomAD v4: 1-77933342-G-A
• COSMIC: COSM3492519 ; COSM3492520
• MyVariant Identifiers: chr1:g.78399027G>A (hg19) ; chr1:g.77933342G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933342G>A , CM000663.2:g.77933342G>A	GRCh38
NC_000001.10:g.78399027G>A , CM000663.1:g.78399027G>A	GRCh37
NC_000001.9:g.78171615G>A	NCBI36
NG_016625.1:g.49828G>A , LRG_442:g.49828G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1114G>A MANE Select	ENSP00000333938.7:p.Gly372Arg
ENST00000330010.12:c.922G>A	ENSP00000327363.8:p.Gly308Arg
ENST00000334785.11:c.1114G>A	ENSP00000333938.7:p.Gly372Arg
ENST00000342754.5:c.813G>A
ENST00000401035.7:c.922G>A	ENSP00000383814.3:p.Gly308Arg
ENST00000440324.5:c.1072G>A	ENSP00000411902.1:p.Gly358Arg
ENST00000464998.1:n.574G>A
ENST00000480732.2:n.688G>A
NM_001172309.1:c.922G>A	NP_001165780.1:p.Gly308Arg
NM_144573.3:c.1114G>A , LRG_442t1:c.1114G>A	NP_653174.3:p.Gly372Arg
XM_005271322.2:c.1114G>A	XP_005271379.1:p.Gly372Arg
XM_005271323.2:c.1072G>A	XP_005271380.1:p.Gly358Arg
XM_005271324.3:c.922G>A	XP_005271381.1:p.Gly308Arg
XM_005271325.2:c.1114G>A	XP_005271382.1:p.Gly372Arg
XM_005271326.2:c.880G>A	XP_005271383.1:p.Gly294Arg
XM_005271327.2:c.697G>A	XP_005271384.1:p.Gly233Arg
XM_005271322.4:c.1114G>A	XP_005271379.1:p.Gly372Arg
XM_005271323.4:c.1072G>A	XP_005271380.1:p.Gly358Arg
XM_005271324.5:c.922G>A	XP_005271381.1:p.Gly308Arg
XM_005271325.4:c.1114G>A	XP_005271382.1:p.Gly372Arg
XM_005271326.4:c.880G>A	XP_005271383.1:p.Gly294Arg
XM_005271327.4:c.697G>A	XP_005271384.1:p.Gly233Arg
NM_001172309.2:c.922G>A	NP_001165780.1:p.Gly308Arg
NM_144573.4:c.1114G>A MANE Select	NP_653174.3:p.Gly372Arg