Canonical Allele Identifier: CA1144241650
Gene: MFN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12009221_12009243delinsGGGAGAGGGAGCGGGAGAGGGAG , CM000663.2:g.12009221_12009243delinsGGGAGAGGGAGCGGGAGAGGGAG GRCh38
NC_000001.10:g.12069278_12069300delinsGGGAGAGGGAGCGGGAGAGGGAG , CM000663.1:g.12069278_12069300delinsGGGAGAGGGAGCGGGAGAGGGAG GRCh37
NC_000001.9:g.11991865_11991887delinsGGGAGAGGGAGCGGGAGAGGGAG NCBI36
NG_007945.1:g.34041_34063delinsGGGAGAGGGAGCGGGAGAGGGAG , LRG_255:g.34041_34063delinsGGGAGAGGGAGCGGGAGAGGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000235329.10:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG MANE Select ENSP00000235329.5:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000674548.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502185.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000674658.1:c.1725-371_1725-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502334.1:n.1725-371_1725-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000674817.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502151.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000674910.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000501716.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000675053.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000501646.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000675113.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502623.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000675231.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502404.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000675298.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000501839.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000675404.1:n.2305-371_2305-349delinsGGGAGAGGGAGCGGGAGAGGGAG
ENST00000675483.1:n.2198-371_2198-349delinsGGGAGAGGGAGCGGGAGAGGGAG
ENST00000675512.1:c.*2072-371_*2072-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502630.1:n.*2072-371_*2072-349delinsGGGAGAGGGAGCGGGA...
ENST00000675528.1:n.1561-371_1561-349delinsGGGAGAGGGAGCGGGAGAGGGAG
ENST00000675817.1:c.2202-371_2202-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502422.1:n.2202-371_2202-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000675872.1:n.2430-371_2430-349delinsGGGAGAGGGAGCGGGAGAGGGAG
ENST00000675919.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000501776.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000675959.1:n.2576-371_2576-349delinsGGGAGAGGGAGCGGGAGAGGGAG
ENST00000675987.1:c.*43-371_*43-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502145.1:n.*43-371_*43-349delinsGGGAGAGGGAGCGGGAGAGG...
ENST00000676293.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502362.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000676295.1:n.483-371_483-349delinsGGGAGAGGGAGCGGGAGAGGGAG
ENST00000676426.1:c.*1070-371_*1070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000502359.1:n.*1070-371_*1070-349delinsGGGAGAGGGAGCGGGA...
ENST00000235329.9:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000235329.5:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
ENST00000444836.5:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG ENSP00000416338.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGA...
NM_001127660.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG NP_001121132.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
NM_014874.3:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG , LRG_255t1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG NP_055689.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG
XM_005263543.2:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_005263600.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
XM_005263545.2:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_005263602.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
XM_005263547.2:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_005263604.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
XM_005263548.2:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_005263605.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
XM_005263543.3:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_005263600.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
XM_005263545.3:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_005263602.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
XM_005263547.3:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_005263604.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
XM_005263548.3:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_005263605.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
XM_024451299.1:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG XP_024307067.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...
NM_014874.4:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG MANE Select NP_055689.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG
NM_001127660.2:c.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGGAG NP_001121132.1:n.2070-371_2070-349delinsGGGAGAGGGAGCGGGAGAGGG...