Canonical Allele Identifier: CA185831

Gene: NEXN

Linked Data

• ClinVar Variation Id: 180108
• ClinVar RCV Id: RCV000156912 ; RCV000157392 ; RCV000869575 ; RCV001456331 ; RCV002444647
• dbSNP Id: rs727505353
• ExAC: 1:78394996 G / A
• gnomAD v2: 1-78394996-G-A
• gnomAD v3: 1-77929311-G-A
• gnomAD v4: 1-77929311-G-A
• MyVariant Identifiers: chr1:g.78394996G>A (hg19) ; chr1:g.77929311G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77929311G>A , CM000663.2:g.77929311G>A	GRCh38
NC_000001.10:g.78394996G>A , CM000663.1:g.78394996G>A	GRCh37
NC_000001.9:g.78167584G>A	NCBI36
NG_016625.1:g.45797G>A , LRG_442:g.45797G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.865-5G>A MANE Select	ENSP00000333938.7:n.865-5G>A
ENST00000330010.12:c.673-5G>A	ENSP00000327363.8:n.673-5G>A
ENST00000334785.11:c.865-5G>A	ENSP00000333938.7:n.865-5G>A
ENST00000342754.5:c.564-5G>A
ENST00000401035.7:c.673-5G>A	ENSP00000383814.3:n.673-5G>A
ENST00000440324.5:c.823-5G>A	ENSP00000411902.1:n.823-5G>A
ENST00000464998.1:n.325-5G>A
NM_001172309.1:c.673-5G>A	NP_001165780.1:n.673-5G>A
NM_144573.3:c.865-5G>A , LRG_442t1:c.865-5G>A	NP_653174.3:n.865-5G>A
XM_005271322.2:c.865-5G>A	XP_005271379.1:n.865-5G>A
XM_005271323.2:c.823-5G>A	XP_005271380.1:n.823-5G>A
XM_005271324.3:c.673-5G>A	XP_005271381.1:n.673-5G>A
XM_005271325.2:c.865-5G>A	XP_005271382.1:n.865-5G>A
XM_005271326.2:c.631-5G>A	XP_005271383.1:n.631-5G>A
XM_005271327.2:c.448-5G>A	XP_005271384.1:n.448-5G>A
XM_005271322.4:c.865-5G>A	XP_005271379.1:n.865-5G>A
XM_005271323.4:c.823-5G>A	XP_005271380.1:n.823-5G>A
XM_005271324.5:c.673-5G>A	XP_005271381.1:n.673-5G>A
XM_005271325.4:c.865-5G>A	XP_005271382.1:n.865-5G>A
XM_005271326.4:c.631-5G>A	XP_005271383.1:n.631-5G>A
XM_005271327.4:c.448-5G>A	XP_005271384.1:n.448-5G>A
NM_001172309.2:c.673-5G>A	NP_001165780.1:n.673-5G>A
NM_144573.4:c.865-5G>A MANE Select	NP_653174.3:n.865-5G>A