Canonical Allele Identifier: CA18013072

Gene: MFN2

Linked Data

• dbSNP Id: rs756517155
• MyVariant Identifiers: chr1:g.12066749_12066750insGGTCAGTGACCA (hg19) ; chr1:g.12006692_12006693insGGTCAGTGACCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12006694_12006705dup , CM000663.2:g.12006694_12006705dup	GRCh38
NC_000001.10:g.12066751_12066762dup , CM000663.1:g.12066751_12066762dup	GRCh37
NC_000001.9:g.11989338_11989349dup	NCBI36
NG_007945.1:g.31514_31525dup , LRG_255:g.31514_31525dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.1872+1_1872+12dup
ENST00000674548.1:c.1872+1_1872+12dup
ENST00000674658.1:c.1527+1_1527+12dup
ENST00000674817.1:c.1872+1_1872+12dup
ENST00000674910.1:c.1872+1_1872+12dup
ENST00000675053.1:c.1872+1_1872+12dup
ENST00000675113.1:c.1872+1_1872+12dup
ENST00000675231.1:c.1872+1_1872+12dup
ENST00000675298.1:c.1872+1_1872+12dup
ENST00000675404.1:n.2107+1_2107+12dup
ENST00000675483.1:n.2000+1_2000+12dup
ENST00000675512.1:c.*1874+1_*1874+12dup
ENST00000675528.1:n.1363+1_1363+12dup
ENST00000675817.1:c.2004+1_2004+12dup
ENST00000675872.1:n.2232+1_2232+12dup
ENST00000675919.1:c.1872+1_1872+12dup
ENST00000675959.1:n.2378+1_2378+12dup
ENST00000675987.1:c.1872+1_1872+12dup
ENST00000676293.1:c.1872+1_1872+12dup
ENST00000676426.1:c.*872+1_*872+12dup
ENST00000235329.9:c.1872+1_1872+12dup
ENST00000444836.5:c.1872+1_1872+12dup
NM_001127660.1:c.1872+1_1872+12dup
NM_014874.3:c.1872+1_1872+12dup , LRG_255t1:c.1872+1_1872+12dup
XM_005263543.2:c.1872+1_1872+12dup
XM_005263545.2:c.1872+1_1872+12dup
XM_005263547.2:c.1872+1_1872+12dup
XM_005263548.2:c.1872+1_1872+12dup
XM_005263543.3:c.1872+1_1872+12dup
XM_005263545.3:c.1872+1_1872+12dup
XM_005263547.3:c.1872+1_1872+12dup
XM_005263548.3:c.1872+1_1872+12dup
XM_024451299.1:c.1872+1_1872+12dup
NM_014874.4:c.1872+1_1872+12dup
NM_001127660.2:c.1872+1_1872+12dup