Canonical Allele Identifier: CA338453290

Gene: MFN2

Linked Data

• ClinVar Variation Id: 2916039
• ClinVar RCV Id: RCV003745229
• MyVariant Identifiers: chr1:g.12069749C>G (hg19) ; chr1:g.12009692C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009692C>G , CM000663.2:g.12009692C>G	GRCh38
NC_000001.10:g.12069749C>G , CM000663.1:g.12069749C>G	GRCh37
NC_000001.9:g.11992336C>G	NCBI36
NG_007945.1:g.34512C>G , LRG_255:g.34512C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2170C>G MANE Select	ENSP00000235329.5:p.Leu724Val
ENST00000674548.1:c.2170C>G	ENSP00000502185.1:p.Leu724Val
ENST00000674658.1:c.1825C>G	ENSP00000502334.1:p.Leu609Val
ENST00000674817.1:c.2170C>G	ENSP00000502151.1:p.Leu724Val
ENST00000674910.1:c.2170C>G	ENSP00000501716.1:p.Leu724Val
ENST00000675043.1:n.138C>G
ENST00000675053.1:c.2170C>G	ENSP00000501646.1:p.Leu724Val
ENST00000675113.1:c.2170C>G	ENSP00000502623.1:p.Leu724Val
ENST00000675231.1:c.2170C>G	ENSP00000502404.1:p.Leu724Val
ENST00000675298.1:c.2170C>G	ENSP00000501839.1:p.Leu724Val
ENST00000675404.1:n.2405C>G
ENST00000675483.1:n.2298C>G
ENST00000675512.1:c.*2172C>G	ENSP00000502630.1:n.*2172C>G
ENST00000675528.1:n.1661C>G
ENST00000675817.1:c.2302C>G	ENSP00000502422.1:p.Leu768Val
ENST00000675872.1:n.2530C>G
ENST00000675919.1:c.2170C>G	ENSP00000501776.1:p.Leu724Val
ENST00000675959.1:n.2676C>G
ENST00000675987.1:c.*143C>G	ENSP00000502145.1:n.*143C>G
ENST00000676293.1:c.2170C>G	ENSP00000502362.1:p.Leu724Val
ENST00000676295.1:n.583C>G
ENST00000676426.1:c.*1170C>G	ENSP00000502359.1:n.*1170C>G
ENST00000235329.9:c.2170C>G	ENSP00000235329.5:p.Leu724Val
ENST00000444836.5:c.2170C>G	ENSP00000416338.1:p.Leu724Val
NM_001127660.1:c.2170C>G	NP_001121132.1:p.Leu724Val
NM_014874.3:c.2170C>G , LRG_255t1:c.2170C>G	NP_055689.1:p.Leu724Val
XM_005263543.2:c.2170C>G	XP_005263600.1:p.Leu724Val
XM_005263545.2:c.2170C>G	XP_005263602.1:p.Leu724Val
XM_005263547.2:c.2170C>G	XP_005263604.1:p.Leu724Val
XM_005263548.2:c.2170C>G	XP_005263605.1:p.Leu724Val
XM_005263543.3:c.2170C>G	XP_005263600.1:p.Leu724Val
XM_005263545.3:c.2170C>G	XP_005263602.1:p.Leu724Val
XM_005263547.3:c.2170C>G	XP_005263604.1:p.Leu724Val
XM_005263548.3:c.2170C>G	XP_005263605.1:p.Leu724Val
XM_024451299.1:c.2170C>G	XP_024307067.1:p.Leu724Val
NM_014874.4:c.2170C>G MANE Select	NP_055689.1:p.Leu724Val
NM_001127660.2:c.2170C>G	NP_001121132.1:p.Leu724Val