Canonical Allele Identifier: CA3044621124

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11998880_11998988del , CM000663.2:g.11998880_11998988del	GRCh38
NC_000001.10:g.12058937_12059045del , CM000663.1:g.12058937_12059045del	GRCh37
NC_000001.9:g.11981524_11981632del	NCBI36
NG_007945.1:g.23700_23808del , LRG_255:g.23700_23808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.708+2_709del
ENST00000674548.1:c.708+2_709del
ENST00000674658.1:c.363+2_364del
ENST00000674706.1:n.1147+2_1148del
ENST00000674817.1:c.708+2_709del
ENST00000674910.1:c.708+2_709del
ENST00000675053.1:c.708+2_709del
ENST00000675113.1:c.708+2_709del
ENST00000675194.1:n.1133+2_1134del
ENST00000675231.1:c.708+2_709del
ENST00000675298.1:c.708+2_709del
ENST00000675374.1:n.400_508del
ENST00000675483.1:n.836+2_837del
ENST00000675512.1:c.*710+2_*711del
ENST00000675528.1:n.199+2_200del
ENST00000675817.1:c.708+2_709del
ENST00000675872.1:n.961_1069del
ENST00000675919.1:c.708+2_709del
ENST00000675959.1:n.1107_1215del
ENST00000675987.1:c.708+2_709del
ENST00000676293.1:c.708+2_709del
ENST00000676426.1:c.599+1459_599+1567del	ENSP00000502359.1:n.599+1459_599+1567del
ENST00000235329.9:c.708+2_709del
ENST00000444836.5:c.708+2_709del
NM_001127660.1:c.708+2_709del
NM_014874.3:c.708+2_709del , LRG_255t1:c.708+2_709del
XM_005263543.2:c.708+2_709del
XM_005263545.2:c.708+2_709del
XM_005263547.2:c.708+2_709del
XM_005263548.2:c.708+2_709del
XM_005263543.3:c.708+2_709del
XM_005263545.3:c.708+2_709del
XM_005263547.3:c.708+2_709del
XM_005263548.3:c.708+2_709del
XM_024451299.1:c.708+2_709del
NM_014874.4:c.708+2_709del
NM_001127660.2:c.708+2_709del