Canonical Allele Identifier: CA279075

Gene: MFN2

Linked Data

• ClinVar Variation Id: 217164
• ClinVar RCV Id: RCV000201063 ; RCV000235729 ; RCV000653851 ; RCV003338460
• dbSNP Id: rs863224970
• MyVariant Identifiers: chr1:g.12057373A>G (hg19) ; chr1:g.11997316A>G (hg38)
• PubMed: PMID:16714318 ; PMID:16835246 ; PMID:17309650 ; PMID:24819634

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11997316A>G , CM000663.2:g.11997316A>G	GRCh38
NC_000001.10:g.12057373A>G , CM000663.1:g.12057373A>G	GRCh37
NC_000001.9:g.11979960A>G	NCBI36
NG_007945.1:g.22136A>G , LRG_255:g.22136A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.494A>G MANE Select	ENSP00000235329.5:p.His165Arg
ENST00000674548.1:c.494A>G	ENSP00000502185.1:p.His165Arg
ENST00000674658.1:c.149A>G	ENSP00000502334.1:p.His50Arg
ENST00000674706.1:n.933A>G
ENST00000674817.1:c.494A>G	ENSP00000502151.1:p.His165Arg
ENST00000674910.1:c.494A>G	ENSP00000501716.1:p.His165Arg
ENST00000675053.1:c.494A>G	ENSP00000501646.1:p.His165Arg
ENST00000675113.1:c.494A>G	ENSP00000502623.1:p.His165Arg
ENST00000675194.1:n.919A>G
ENST00000675231.1:c.494A>G	ENSP00000502404.1:p.His165Arg
ENST00000675298.1:c.494A>G	ENSP00000501839.1:p.His165Arg
ENST00000675374.1:n.184A>G
ENST00000675483.1:n.622A>G
ENST00000675512.1:c.*496A>G	ENSP00000502630.1:n.*496A>G
ENST00000675817.1:c.494A>G	ENSP00000502422.1:p.His165Arg
ENST00000675872.1:n.745A>G
ENST00000675919.1:c.494A>G	ENSP00000501776.1:p.His165Arg
ENST00000675959.1:n.891A>G
ENST00000675987.1:c.494A>G	ENSP00000502145.1:p.His165Arg
ENST00000676293.1:c.494A>G	ENSP00000502362.1:p.His165Arg
ENST00000676426.1:c.494A>G	ENSP00000502359.1:p.His165Arg
ENST00000235329.9:c.494A>G	ENSP00000235329.5:p.His165Arg
ENST00000444836.5:c.494A>G	ENSP00000416338.1:p.His165Arg
NM_001127660.1:c.494A>G	NP_001121132.1:p.His165Arg
NM_014874.3:c.494A>G , LRG_255t1:c.494A>G	NP_055689.1:p.His165Arg
XM_005263543.2:c.494A>G	XP_005263600.1:p.His165Arg
XM_005263545.2:c.494A>G	XP_005263602.1:p.His165Arg
XM_005263547.2:c.494A>G	XP_005263604.1:p.His165Arg
XM_005263548.2:c.494A>G	XP_005263605.1:p.His165Arg
XM_005263543.3:c.494A>G	XP_005263600.1:p.His165Arg
XM_005263545.3:c.494A>G	XP_005263602.1:p.His165Arg
XM_005263547.3:c.494A>G	XP_005263604.1:p.His165Arg
XM_005263548.3:c.494A>G	XP_005263605.1:p.His165Arg
XM_024451299.1:c.494A>G	XP_024307067.1:p.His165Arg
NM_014874.4:c.494A>G MANE Select	NP_055689.1:p.His165Arg
NM_001127660.2:c.494A>G	NP_001121132.1:p.His165Arg