Canonical Allele Identifier: CA1153915708

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11998756_11998758delinsCCT , CM000663.2:g.11998756_11998758delinsCCT	GRCh38
NC_000001.10:g.12058813_12058815delinsCCT , CM000663.1:g.12058813_12058815delinsCCT	GRCh37
NC_000001.9:g.11981400_11981402delinsCCT	NCBI36
NG_007945.1:g.23576_23578delinsCCT , LRG_255:g.23576_23578delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.600-14_600-12delinsCCT MANE Select	ENSP00000235329.5:n.600-14_600-12delinsCCT
ENST00000674548.1:c.600-14_600-12delinsCCT	ENSP00000502185.1:n.600-14_600-12delinsCCT
ENST00000674658.1:c.255-14_255-12delinsCCT	ENSP00000502334.1:n.255-14_255-12delinsCCT
ENST00000674706.1:n.1039-14_1039-12delinsCCT
ENST00000674817.1:c.600-14_600-12delinsCCT	ENSP00000502151.1:n.600-14_600-12delinsCCT
ENST00000674910.1:c.600-14_600-12delinsCCT	ENSP00000501716.1:n.600-14_600-12delinsCCT
ENST00000675053.1:c.600-14_600-12delinsCCT	ENSP00000501646.1:n.600-14_600-12delinsCCT
ENST00000675113.1:c.600-14_600-12delinsCCT	ENSP00000502623.1:n.600-14_600-12delinsCCT
ENST00000675194.1:n.1025-14_1025-12delinsCCT
ENST00000675231.1:c.600-14_600-12delinsCCT	ENSP00000502404.1:n.600-14_600-12delinsCCT
ENST00000675298.1:c.600-14_600-12delinsCCT	ENSP00000501839.1:n.600-14_600-12delinsCCT
ENST00000675374.1:n.290-14_290-12delinsCCT
ENST00000675483.1:n.728-14_728-12delinsCCT
ENST00000675512.1:c.*602-14_*602-12delinsCCT	ENSP00000502630.1:n.*602-14_*602-12delinsCCT
ENST00000675528.1:n.77_79delinsCCT
ENST00000675817.1:c.600-14_600-12delinsCCT	ENSP00000502422.1:n.600-14_600-12delinsCCT
ENST00000675872.1:n.851-14_851-12delinsCCT
ENST00000675919.1:c.600-14_600-12delinsCCT	ENSP00000501776.1:n.600-14_600-12delinsCCT
ENST00000675959.1:n.997-14_997-12delinsCCT
ENST00000675987.1:c.600-14_600-12delinsCCT	ENSP00000502145.1:n.600-14_600-12delinsCCT
ENST00000676293.1:c.600-14_600-12delinsCCT	ENSP00000502362.1:n.600-14_600-12delinsCCT
ENST00000676426.1:c.599+1335_599+1337delinsCCT	ENSP00000502359.1:n.599+1335_599+1337delinsCCT
ENST00000235329.9:c.600-14_600-12delinsCCT	ENSP00000235329.5:n.600-14_600-12delinsCCT
ENST00000444836.5:c.600-14_600-12delinsCCT	ENSP00000416338.1:n.600-14_600-12delinsCCT
NM_001127660.1:c.600-14_600-12delinsCCT	NP_001121132.1:n.600-14_600-12delinsCCT
NM_014874.3:c.600-14_600-12delinsCCT , LRG_255t1:c.600-14_600-12delinsCCT	NP_055689.1:n.600-14_600-12delinsCCT
XM_005263543.2:c.600-14_600-12delinsCCT	XP_005263600.1:n.600-14_600-12delinsCCT
XM_005263545.2:c.600-14_600-12delinsCCT	XP_005263602.1:n.600-14_600-12delinsCCT
XM_005263547.2:c.600-14_600-12delinsCCT	XP_005263604.1:n.600-14_600-12delinsCCT
XM_005263548.2:c.600-14_600-12delinsCCT	XP_005263605.1:n.600-14_600-12delinsCCT
XM_005263543.3:c.600-14_600-12delinsCCT	XP_005263600.1:n.600-14_600-12delinsCCT
XM_005263545.3:c.600-14_600-12delinsCCT	XP_005263602.1:n.600-14_600-12delinsCCT
XM_005263547.3:c.600-14_600-12delinsCCT	XP_005263604.1:n.600-14_600-12delinsCCT
XM_005263548.3:c.600-14_600-12delinsCCT	XP_005263605.1:n.600-14_600-12delinsCCT
XM_024451299.1:c.600-14_600-12delinsCCT	XP_024307067.1:n.600-14_600-12delinsCCT
NM_014874.4:c.600-14_600-12delinsCCT MANE Select	NP_055689.1:n.600-14_600-12delinsCCT
NM_001127660.2:c.600-14_600-12delinsCCT	NP_001121132.1:n.600-14_600-12delinsCCT