Canonical Allele Identifier: CA2741808818
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30737

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11998770_11999095del , CM000663.2:g.11998770_11999095del GRCh38
NC_000001.10:g.12058827_12059152del , CM000663.1:g.12058827_12059152del GRCh37
NC_000001.9:g.11981414_11981739del NCBI36
NG_007945.1:g.23590_23915del , LRG_255:g.23590_23915del

Transcript Alleles

HGVS Amino-acid change
ENST00000235329.10:c.600_816del
ENST00000674548.1:c.600_816del
ENST00000674658.1:c.255_471del
ENST00000674706.1:n.1039_1255del
ENST00000674817.1:c.600_816del
ENST00000674910.1:c.600_816del
ENST00000675053.1:c.600_816del
ENST00000675113.1:c.600_816del
ENST00000675194.1:n.1025_1241del
ENST00000675231.1:c.600_816del
ENST00000675298.1:c.600_816del
ENST00000675483.1:n.728_944del
ENST00000675512.1:c.*602_*818del
ENST00000675528.1:n.91_307del
ENST00000675817.1:c.600_816del
ENST00000675872.1:n.851_1176del
ENST00000675919.1:c.600_816del
ENST00000675959.1:n.997_1322del
ENST00000675987.1:c.600_816del
ENST00000676293.1:c.600_816del
ENST00000676426.1:c.599+1349_599+1674del ENSP00000502359.1:n.599+1349_599+1674del
ENST00000235329.9:c.600_816del
ENST00000444836.5:c.600_816del
NM_001127660.1:c.600_816del
NM_014874.3:c.600_816del , LRG_255t1:c.600_816del
XM_005263543.2:c.600_816del
XM_005263545.2:c.600_816del
XM_005263547.2:c.600_816del
XM_005263548.2:c.600_816del
XM_005263543.3:c.600_816del
XM_005263545.3:c.600_816del
XM_005263547.3:c.600_816del
XM_005263548.3:c.600_816del
XM_024451299.1:c.600_816del
NM_014874.4:c.600_816del
NM_001127660.2:c.600_816del