Canonical Allele Identifier: CA338461834

Gene: MFN2

Linked Data

• dbSNP Id: rs1218698482
• gnomAD v2: 1-12052662-C-A
• gnomAD v4: 1-11992605-C-A
• MyVariant Identifiers: chr1:g.12052662C>A (hg19) ; chr1:g.11992605C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11992605C>A , CM000663.2:g.11992605C>A	GRCh38
NC_000001.10:g.12052662C>A , CM000663.1:g.12052662C>A	GRCh37
NC_000001.9:g.11975249C>A	NCBI36
NG_007945.1:g.17425C>A , LRG_255:g.17425C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.226C>A MANE Select	ENSP00000235329.5:p.Leu76Met
ENST00000412236.2:c.226C>A	ENSP00000412023.1:p.Leu76Met
ENST00000674548.1:c.226C>A	ENSP00000502185.1:p.Leu76Met
ENST00000674658.1:c.-34-3551C>A	ENSP00000502334.1:n.-34-3551C>A
ENST00000674706.1:n.665C>A
ENST00000674817.1:c.226C>A	ENSP00000502151.1:p.Leu76Met
ENST00000674910.1:c.226C>A	ENSP00000501716.1:p.Leu76Met
ENST00000675053.1:c.226C>A	ENSP00000501646.1:p.Leu76Met
ENST00000675113.1:c.226C>A	ENSP00000502623.1:p.Leu76Met
ENST00000675194.1:n.651C>A
ENST00000675231.1:c.226C>A	ENSP00000502404.1:p.Leu76Met
ENST00000675298.1:c.226C>A	ENSP00000501839.1:p.Leu76Met
ENST00000675483.1:n.354C>A
ENST00000675512.1:c.*228C>A	ENSP00000502630.1:n.*228C>A
ENST00000675530.1:c.226C>A	ENSP00000501972.1:p.Leu76Met
ENST00000675817.1:c.226C>A	ENSP00000502422.1:p.Leu76Met
ENST00000675872.1:n.477C>A
ENST00000675919.1:c.226C>A	ENSP00000501776.1:p.Leu76Met
ENST00000675959.1:n.623C>A
ENST00000675987.1:c.226C>A	ENSP00000502145.1:p.Leu76Met
ENST00000676293.1:c.226C>A	ENSP00000502362.1:p.Leu76Met
ENST00000676369.1:c.226C>A	ENSP00000502005.1:p.Leu76Met
ENST00000676426.1:c.226C>A	ENSP00000502359.1:p.Leu76Met
ENST00000235329.9:c.226C>A	ENSP00000235329.5:p.Leu76Met
ENST00000412236.1:c.226C>A	ENSP00000412023.1:p.Leu76Met
ENST00000444836.5:c.226C>A	ENSP00000416338.1:p.Leu76Met
ENST00000497302.1:n.610C>A
NM_001127660.1:c.226C>A	NP_001121132.1:p.Leu76Met
NM_014874.3:c.226C>A , LRG_255t1:c.226C>A	NP_055689.1:p.Leu76Met
XM_005263543.2:c.226C>A	XP_005263600.1:p.Leu76Met
XM_005263545.2:c.226C>A	XP_005263602.1:p.Leu76Met
XM_005263547.2:c.226C>A	XP_005263604.1:p.Leu76Met
XM_005263548.2:c.226C>A	XP_005263605.1:p.Leu76Met
XM_005263543.3:c.226C>A	XP_005263600.1:p.Leu76Met
XM_005263545.3:c.226C>A	XP_005263602.1:p.Leu76Met
XM_005263547.3:c.226C>A	XP_005263604.1:p.Leu76Met
XM_005263548.3:c.226C>A	XP_005263605.1:p.Leu76Met
XM_024451299.1:c.226C>A	XP_024307067.1:p.Leu76Met
NM_014874.4:c.226C>A MANE Select	NP_055689.1:p.Leu76Met
NM_001127660.2:c.226C>A	NP_001121132.1:p.Leu76Met