Canonical Allele Identifier: CA2742488077
Gene: MFN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11999061_11999062insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC , CM000663.2:g.11999061_11999062insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC GRCh38
NC_000001.10:g.12059118_12059119insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC , CM000663.1:g.12059118_12059119insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC GRCh37
NC_000001.9:g.11981705_11981706insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC NCBI36
NG_007945.1:g.23881_23882insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC , LRG_255:g.23881_23882insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000235329.10:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC MANE Select ENSP00000235329.5:p.Asp261GlufsTer?
ENST00000674548.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502185.1:p.Asp261GlufsTer?
ENST00000674658.1:c.437_438insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502334.1:p.Asp146GlufsTer?
ENST00000674706.1:n.1221_1222insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC
ENST00000674817.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502151.1:p.Asp261GlufsTer?
ENST00000674910.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000501716.1:p.Asp261GlufsTer?
ENST00000675053.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000501646.1:p.Asp261GlufsTer?
ENST00000675113.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502623.1:p.Asp261GlufsTer?
ENST00000675194.1:n.1207_1208insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC
ENST00000675231.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502404.1:p.Asp261GlufsTer?
ENST00000675298.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000501839.1:p.Asp261GlufsTer?
ENST00000675374.1:n.581_582insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC
ENST00000675483.1:n.910_911insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC
ENST00000675512.1:c.*784_*785insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502630.1:n.*784_*785insGTTCTTTCAGTTCGCCCAACCAAGACTCG...
ENST00000675528.1:n.273_274insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC
ENST00000675817.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502422.1:p.Asp261GlufsTer?
ENST00000675872.1:n.1142_1143insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC
ENST00000675919.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000501776.1:p.Asp261GlufsTer?
ENST00000675959.1:n.1288_1289insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC
ENST00000675987.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502145.1:p.Asp261GlufsTer?
ENST00000676293.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502362.1:p.Asp261GlufsTer?
ENST00000676426.1:c.599+1640_599+1641insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000502359.1:n.599+1640_599+1641insGTTCTTTCAGTTCGCCCAACC...
ENST00000235329.9:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000235329.5:p.Asp261GlufsTer?
ENST00000444836.5:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC ENSP00000416338.1:p.Asp261GlufsTer?
NM_001127660.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC NP_001121132.1:p.Asp261GlufsTer?
NM_014874.3:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC , LRG_255t1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC NP_055689.1:p.Asp261GlufsTer?
XM_005263543.2:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_005263600.1:p.Asp261GlufsTer?
XM_005263545.2:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_005263602.1:p.Asp261GlufsTer?
XM_005263547.2:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_005263604.1:p.Asp261GlufsTer?
XM_005263548.2:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_005263605.1:p.Asp261GlufsTer?
XM_005263543.3:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_005263600.1:p.Asp261GlufsTer?
XM_005263545.3:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_005263602.1:p.Asp261GlufsTer?
XM_005263547.3:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_005263604.1:p.Asp261GlufsTer?
XM_005263548.3:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_005263605.1:p.Asp261GlufsTer?
XM_024451299.1:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC XP_024307067.1:p.Asp261GlufsTer?
NM_014874.4:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC MANE Select NP_055689.1:p.Asp261GlufsTer?
NM_001127660.2:c.782_783insGTTCTTTCAGTTCGCCCAACCAAGACTCGATTTGGTTTTTTTCC NP_001121132.1:p.Asp261GlufsTer?