Canonical Allele Identifier: CA918562

Gene: NEXN

Linked Data

• ClinVar Variation Id: 1768535
• ClinVar RCV Id: RCV002387443
• dbSNP Id: rs771890063
• ExAC: 1:78383321 A / G
• gnomAD v2: 1-78383321-A-G
• gnomAD v3: 1-77917636-A-G
• gnomAD v4: 1-77917636-A-G
• MyVariant Identifiers: chr1:g.78383321A>G (hg19) ; chr1:g.77917636A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77917636A>G , CM000663.2:g.77917636A>G	GRCh38
NC_000001.10:g.78383321A>G , CM000663.1:g.78383321A>G	GRCh37
NC_000001.9:g.78155909A>G	NCBI36
NG_016625.1:g.34122A>G , LRG_442:g.34122A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.98A>G MANE Select	ENSP00000333938.7:p.Asp33Gly
ENST00000330010.12:c.28-324A>G	ENSP00000327363.8:n.28-324A>G
ENST00000334785.11:c.98A>G	ENSP00000333938.7:p.Asp33Gly
ENST00000401035.7:c.28-324A>G	ENSP00000383814.3:n.28-324A>G
ENST00000440324.5:c.98A>G	ENSP00000411902.1:p.Asp33Gly
NM_001172309.1:c.28-324A>G	NP_001165780.1:n.28-324A>G
NM_144573.3:c.98A>G , LRG_442t1:c.98A>G	NP_653174.3:p.Asp33Gly
XM_005271322.2:c.98A>G	XP_005271379.1:p.Asp33Gly
XM_005271323.2:c.98A>G	XP_005271380.1:p.Asp33Gly
XM_005271324.3:c.28-324A>G	XP_005271381.1:n.28-324A>G
XM_005271325.2:c.98A>G	XP_005271382.1:p.Asp33Gly
XM_005271326.2:c.28-324A>G	XP_005271383.1:n.28-324A>G
XM_005271327.2:c.98A>G	XP_005271384.1:p.Asp33Gly
XM_005271322.4:c.98A>G	XP_005271379.1:p.Asp33Gly
XM_005271323.4:c.98A>G	XP_005271380.1:p.Asp33Gly
XM_005271324.5:c.28-324A>G	XP_005271381.1:n.28-324A>G
XM_005271325.4:c.98A>G	XP_005271382.1:p.Asp33Gly
XM_005271326.4:c.28-324A>G	XP_005271383.1:n.28-324A>G
XM_005271327.4:c.98A>G	XP_005271384.1:p.Asp33Gly
NM_001172309.2:c.28-324A>G	NP_001165780.1:n.28-324A>G
NM_144573.4:c.98A>G MANE Select	NP_653174.3:p.Asp33Gly