Canonical Allele Identifier: CA1153916141

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11998886_11998887delinsCT , CM000663.2:g.11998886_11998887delinsCT	GRCh38
NC_000001.10:g.12058943_12058944delinsCT , CM000663.1:g.12058943_12058944delinsCT	GRCh37
NC_000001.9:g.11981530_11981531delinsCT	NCBI36
NG_007945.1:g.23706_23707delinsCT , LRG_255:g.23706_23707delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000235329.10:c.708+8_708+9delinsCT MANE Select	ENSP00000235329.5:n.708+8_708+9delinsCT
ENST00000674548.1:c.708+8_708+9delinsCT	ENSP00000502185.1:n.708+8_708+9delinsCT
ENST00000674658.1:c.363+8_363+9delinsCT	ENSP00000502334.1:n.363+8_363+9delinsCT
ENST00000674706.1:n.1147+8_1147+9delinsCT
ENST00000674817.1:c.708+8_708+9delinsCT	ENSP00000502151.1:n.708+8_708+9delinsCT
ENST00000674910.1:c.708+8_708+9delinsCT	ENSP00000501716.1:n.708+8_708+9delinsCT
ENST00000675053.1:c.708+8_708+9delinsCT	ENSP00000501646.1:n.708+8_708+9delinsCT
ENST00000675113.1:c.708+8_708+9delinsCT	ENSP00000502623.1:n.708+8_708+9delinsCT
ENST00000675194.1:n.1133+8_1133+9delinsCT
ENST00000675231.1:c.708+8_708+9delinsCT	ENSP00000502404.1:n.708+8_708+9delinsCT
ENST00000675298.1:c.708+8_708+9delinsCT	ENSP00000501839.1:n.708+8_708+9delinsCT
ENST00000675374.1:n.406_407delinsCT
ENST00000675483.1:n.836+8_836+9delinsCT
ENST00000675512.1:c.*710+8_*710+9delinsCT	ENSP00000502630.1:n.*710+8_*710+9delinsCT...
ENST00000675528.1:n.199+8_199+9delinsCT
ENST00000675817.1:c.708+8_708+9delinsCT	ENSP00000502422.1:n.708+8_708+9delinsCT
ENST00000675872.1:n.967_968delinsCT
ENST00000675919.1:c.708+8_708+9delinsCT	ENSP00000501776.1:n.708+8_708+9delinsCT
ENST00000675959.1:n.1113_1114delinsCT
ENST00000675987.1:c.708+8_708+9delinsCT	ENSP00000502145.1:n.708+8_708+9delinsCT
ENST00000676293.1:c.708+8_708+9delinsCT	ENSP00000502362.1:n.708+8_708+9delinsCT
ENST00000676426.1:c.599+1465_599+1466delinsCT	ENSP00000502359.1:n.599+1465_599+1466deli...
ENST00000235329.9:c.708+8_708+9delinsCT	ENSP00000235329.5:n.708+8_708+9delinsCT
ENST00000444836.5:c.708+8_708+9delinsCT	ENSP00000416338.1:n.708+8_708+9delinsCT
NM_001127660.1:c.708+8_708+9delinsCT	NP_001121132.1:n.708+8_708+9delinsCT
NM_014874.3:c.708+8_708+9delinsCT , LRG_255t1:c.708+8_708+9delinsCT	NP_055689.1:n.708+8_708+9delinsCT
XM_005263543.2:c.708+8_708+9delinsCT	XP_005263600.1:n.708+8_708+9delinsCT
XM_005263545.2:c.708+8_708+9delinsCT	XP_005263602.1:n.708+8_708+9delinsCT
XM_005263547.2:c.708+8_708+9delinsCT	XP_005263604.1:n.708+8_708+9delinsCT
XM_005263548.2:c.708+8_708+9delinsCT	XP_005263605.1:n.708+8_708+9delinsCT
XM_005263543.3:c.708+8_708+9delinsCT	XP_005263600.1:n.708+8_708+9delinsCT
XM_005263545.3:c.708+8_708+9delinsCT	XP_005263602.1:n.708+8_708+9delinsCT
XM_005263547.3:c.708+8_708+9delinsCT	XP_005263604.1:n.708+8_708+9delinsCT
XM_005263548.3:c.708+8_708+9delinsCT	XP_005263605.1:n.708+8_708+9delinsCT
XM_024451299.1:c.708+8_708+9delinsCT	XP_024307067.1:n.708+8_708+9delinsCT
NM_014874.4:c.708+8_708+9delinsCT MANE Select	NP_055689.1:n.708+8_708+9delinsCT
NM_001127660.2:c.708+8_708+9delinsCT	NP_001121132.1:n.708+8_708+9delinsCT