Canonical Allele Identifier: CA2742489256

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12007258_12007259insT , CM000663.2:g.12007258_12007259insT	GRCh38
NC_000001.10:g.12067315_12067316insT , CM000663.1:g.12067315_12067316insT	GRCh37
NC_000001.9:g.11989902_11989903insT	NCBI36
NG_007945.1:g.32078_32079insT , LRG_255:g.32078_32079insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2069+9_2069+10insT MANE Select	ENSP00000235329.5:n.2069+9_2069+10insT
ENST00000674548.1:c.2069+9_2069+10insT	ENSP00000502185.1:n.2069+9_2069+10insT
ENST00000674658.1:c.1724+9_1724+10insT	ENSP00000502334.1:n.1724+9_1724+10insT
ENST00000674817.1:c.2069+9_2069+10insT	ENSP00000502151.1:n.2069+9_2069+10insT
ENST00000674910.1:c.2069+9_2069+10insT	ENSP00000501716.1:n.2069+9_2069+10insT
ENST00000675053.1:c.2069+9_2069+10insT	ENSP00000501646.1:n.2069+9_2069+10insT
ENST00000675113.1:c.2069+9_2069+10insT	ENSP00000502623.1:n.2069+9_2069+10insT
ENST00000675231.1:c.2069+9_2069+10insT	ENSP00000502404.1:n.2069+9_2069+10insT
ENST00000675298.1:c.2069+9_2069+10insT	ENSP00000501839.1:n.2069+9_2069+10insT
ENST00000675404.1:n.2304+9_2304+10insT
ENST00000675483.1:n.2197+9_2197+10insT
ENST00000675512.1:c.*2071+9_*2071+10insT	ENSP00000502630.1:n.*2071+9_*2071+10insT
ENST00000675528.1:n.1560+9_1560+10insT
ENST00000675817.1:c.2201+9_2201+10insT	ENSP00000502422.1:n.2201+9_2201+10insT
ENST00000675872.1:n.2429+9_2429+10insT
ENST00000675919.1:c.2069+9_2069+10insT	ENSP00000501776.1:n.2069+9_2069+10insT
ENST00000675959.1:n.2575+9_2575+10insT
ENST00000675987.1:c.*5_*6insT	ENSP00000502145.1:n.*5_*6insT
ENST00000676293.1:c.2069+9_2069+10insT	ENSP00000502362.1:n.2069+9_2069+10insT
ENST00000676295.1:n.482+9_482+10insT
ENST00000676426.1:c.*1069+9_*1069+10insT	ENSP00000502359.1:n.*1069+9_*1069+10insT
ENST00000235329.9:c.2069+9_2069+10insT	ENSP00000235329.5:n.2069+9_2069+10insT
ENST00000444836.5:c.2069+9_2069+10insT	ENSP00000416338.1:n.2069+9_2069+10insT
NM_001127660.1:c.2069+9_2069+10insT	NP_001121132.1:n.2069+9_2069+10insT
NM_014874.3:c.2069+9_2069+10insT , LRG_255t1:c.2069+9_2069+10insT	NP_055689.1:n.2069+9_2069+10insT
XM_005263543.2:c.2069+9_2069+10insT	XP_005263600.1:n.2069+9_2069+10insT
XM_005263545.2:c.2069+9_2069+10insT	XP_005263602.1:n.2069+9_2069+10insT
XM_005263547.2:c.2069+9_2069+10insT	XP_005263604.1:n.2069+9_2069+10insT
XM_005263548.2:c.2069+9_2069+10insT	XP_005263605.1:n.2069+9_2069+10insT
XM_005263543.3:c.2069+9_2069+10insT	XP_005263600.1:n.2069+9_2069+10insT
XM_005263545.3:c.2069+9_2069+10insT	XP_005263602.1:n.2069+9_2069+10insT
XM_005263547.3:c.2069+9_2069+10insT	XP_005263604.1:n.2069+9_2069+10insT
XM_005263548.3:c.2069+9_2069+10insT	XP_005263605.1:n.2069+9_2069+10insT
XM_024451299.1:c.2069+9_2069+10insT	XP_024307067.1:n.2069+9_2069+10insT
NM_014874.4:c.2069+9_2069+10insT MANE Select	NP_055689.1:n.2069+9_2069+10insT
NM_001127660.2:c.2069+9_2069+10insT	NP_001121132.1:n.2069+9_2069+10insT