Canonical Allele Identifier: CA1153924022
Gene: MFN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12004737_12004738delinsCG , CM000663.2:g.12004737_12004738delinsCG GRCh38
NC_000001.10:g.12064794_12064795delinsCG , CM000663.1:g.12064794_12064795delinsCG GRCh37
NC_000001.9:g.11987381_11987382delinsCG NCBI36
NG_007945.1:g.29557_29558delinsCG , LRG_255:g.29557_29558delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000235329.10:c.1393-88_1393-87delinsCG MANE Select ENSP00000235329.5:n.1393-88_1393-87delinsCG
ENST00000674548.1:c.1393-88_1393-87delinsCG ENSP00000502185.1:n.1393-88_1393-87delinsCG
ENST00000674658.1:c.1048-88_1048-87delinsCG ENSP00000502334.1:n.1048-88_1048-87delinsCG
ENST00000674817.1:c.1393-88_1393-87delinsCG ENSP00000502151.1:n.1393-88_1393-87delinsCG
ENST00000674910.1:c.1393-88_1393-87delinsCG ENSP00000501716.1:n.1393-88_1393-87delinsCG
ENST00000675053.1:c.1393-88_1393-87delinsCG ENSP00000501646.1:n.1393-88_1393-87delinsCG
ENST00000675113.1:c.1393-88_1393-87delinsCG ENSP00000502623.1:n.1393-88_1393-87delinsCG
ENST00000675231.1:c.1393-88_1393-87delinsCG ENSP00000502404.1:n.1393-88_1393-87delinsCG
ENST00000675298.1:c.1393-88_1393-87delinsCG ENSP00000501839.1:n.1393-88_1393-87delinsCG
ENST00000675404.1:n.1628-88_1628-87delinsCG
ENST00000675483.1:n.1521-88_1521-87delinsCG
ENST00000675512.1:c.*1395-88_*1395-87delinsCG ENSP00000502630.1:n.*1395-88_*1395-87delinsCG
ENST00000675528.1:n.884-88_884-87delinsCG
ENST00000675817.1:c.1525-88_1525-87delinsCG ENSP00000502422.1:n.1525-88_1525-87delinsCG
ENST00000675872.1:n.1753-88_1753-87delinsCG
ENST00000675919.1:c.1393-88_1393-87delinsCG ENSP00000501776.1:n.1393-88_1393-87delinsCG
ENST00000675959.1:n.1899-88_1899-87delinsCG
ENST00000675987.1:c.1393-88_1393-87delinsCG ENSP00000502145.1:n.1393-88_1393-87delinsCG
ENST00000676293.1:c.1393-88_1393-87delinsCG ENSP00000502362.1:n.1393-88_1393-87delinsCG
ENST00000676426.1:c.*393-88_*393-87delinsCG ENSP00000502359.1:n.*393-88_*393-87delinsCG
ENST00000235329.9:c.1393-88_1393-87delinsCG ENSP00000235329.5:n.1393-88_1393-87delinsCG
ENST00000444836.5:c.1393-88_1393-87delinsCG ENSP00000416338.1:n.1393-88_1393-87delinsCG
NM_001127660.1:c.1393-88_1393-87delinsCG NP_001121132.1:n.1393-88_1393-87delinsCG
NM_014874.3:c.1393-88_1393-87delinsCG , LRG_255t1:c.1393-88_1393-87delinsCG NP_055689.1:n.1393-88_1393-87delinsCG
XM_005263543.2:c.1393-88_1393-87delinsCG XP_005263600.1:n.1393-88_1393-87delinsCG
XM_005263545.2:c.1393-88_1393-87delinsCG XP_005263602.1:n.1393-88_1393-87delinsCG
XM_005263547.2:c.1393-88_1393-87delinsCG XP_005263604.1:n.1393-88_1393-87delinsCG
XM_005263548.2:c.1393-88_1393-87delinsCG XP_005263605.1:n.1393-88_1393-87delinsCG
XM_005263543.3:c.1393-88_1393-87delinsCG XP_005263600.1:n.1393-88_1393-87delinsCG
XM_005263545.3:c.1393-88_1393-87delinsCG XP_005263602.1:n.1393-88_1393-87delinsCG
XM_005263547.3:c.1393-88_1393-87delinsCG XP_005263604.1:n.1393-88_1393-87delinsCG
XM_005263548.3:c.1393-88_1393-87delinsCG XP_005263605.1:n.1393-88_1393-87delinsCG
XM_024451299.1:c.1393-88_1393-87delinsCG XP_024307067.1:n.1393-88_1393-87delinsCG
NM_014874.4:c.1393-88_1393-87delinsCG MANE Select NP_055689.1:n.1393-88_1393-87delinsCG
NM_001127660.2:c.1393-88_1393-87delinsCG NP_001121132.1:n.1393-88_1393-87delinsCG