Canonical Allele Identifier: CA918875

Gene: NEXN

Linked Data

• ClinVar Variation Id: 1101985
• ClinVar RCV Id: RCV001425096 ; RCV002395973 ; RCV004531290
• dbSNP Id: rs140900323
• ExAC: 1:78401675 A / G
• gnomAD v2: 1-78401675-A-G
• gnomAD v3: 1-77935990-A-G
• gnomAD v4: 1-77935990-A-G
• MyVariant Identifiers: chr1:g.78401675A>G (hg19) ; chr1:g.77935990A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935990A>G , CM000663.2:g.77935990A>G	GRCh38
NC_000001.10:g.78401675A>G , CM000663.1:g.78401675A>G	GRCh37
NC_000001.9:g.78174263A>G	NCBI36
NG_016625.1:g.52476A>G , LRG_442:g.52476A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1419A>G MANE Select	ENSP00000333938.7:p.Arg473=
ENST00000330010.12:c.1227A>G	ENSP00000327363.8:p.Arg409=
ENST00000334785.11:c.1419A>G	ENSP00000333938.7:p.Arg473=
ENST00000342754.5:c.1118A>G
ENST00000480732.2:n.993A>G
NM_001172309.1:c.1227A>G	NP_001165780.1:p.Arg409=
NM_144573.3:c.1419A>G , LRG_442t1:c.1419A>G	NP_653174.3:p.Arg473=
XM_005271322.2:c.1419A>G	XP_005271379.1:p.Arg473=
XM_005271323.2:c.1377A>G	XP_005271380.1:p.Arg459=
XM_005271324.3:c.1227A>G	XP_005271381.1:p.Arg409=
XM_005271325.2:c.1251+2511A>G	XP_005271382.1:n.1251+2511A>G
XM_005271326.2:c.1185A>G	XP_005271383.1:p.Arg395=
XM_005271327.2:c.1002A>G	XP_005271384.1:p.Arg334=
XM_005271322.4:c.1419A>G	XP_005271379.1:p.Arg473=
XM_005271323.4:c.1377A>G	XP_005271380.1:p.Arg459=
XM_005271324.5:c.1227A>G	XP_005271381.1:p.Arg409=
XM_005271325.4:c.1251+2511A>G	XP_005271382.1:n.1251+2511A>G
XM_005271326.4:c.1185A>G	XP_005271383.1:p.Arg395=
XM_005271327.4:c.1002A>G	XP_005271384.1:p.Arg334=
NM_001172309.2:c.1227A>G	NP_001165780.1:p.Arg409=
NM_144573.4:c.1419A>G MANE Select	NP_653174.3:p.Arg473=