Canonical Allele Identifier: CA1153909308

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11992678_11992679delinsCT , CM000663.2:g.11992678_11992679delinsCT	GRCh38
NC_000001.10:g.12052735_12052736delinsCT , CM000663.1:g.12052735_12052736delinsCT	GRCh37
NC_000001.9:g.11975322_11975323delinsCT	NCBI36
NG_007945.1:g.17498_17499delinsCT , LRG_255:g.17498_17499delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.299_300delinsCT MANE Select	ENSP00000235329.5:p.Ala100=
ENST00000674548.1:c.299_300delinsCT	ENSP00000502185.1:p.Ala100=
ENST00000674658.1:c.-34-3478_-34-3477delinsCT	ENSP00000502334.1:n.-34-3478_-34-3477delinsCT
ENST00000674706.1:n.738_739delinsCT
ENST00000674817.1:c.299_300delinsCT	ENSP00000502151.1:p.Ala100=
ENST00000674910.1:c.299_300delinsCT	ENSP00000501716.1:p.Ala100=
ENST00000675053.1:c.299_300delinsCT	ENSP00000501646.1:p.Ala100=
ENST00000675113.1:c.299_300delinsCT	ENSP00000502623.1:p.Ala100=
ENST00000675194.1:n.724_725delinsCT
ENST00000675231.1:c.299_300delinsCT	ENSP00000502404.1:p.Ala100=
ENST00000675298.1:c.299_300delinsCT	ENSP00000501839.1:p.Ala100=
ENST00000675483.1:n.427_428delinsCT
ENST00000675512.1:c.*301_*302delinsCT	ENSP00000502630.1:n.*301_*302delinsCT
ENST00000675817.1:c.299_300delinsCT	ENSP00000502422.1:p.Ala100=
ENST00000675872.1:n.550_551delinsCT
ENST00000675919.1:c.299_300delinsCT	ENSP00000501776.1:p.Ala100=
ENST00000675959.1:n.696_697delinsCT
ENST00000675987.1:c.299_300delinsCT	ENSP00000502145.1:p.Ala100=
ENST00000676293.1:c.299_300delinsCT	ENSP00000502362.1:p.Ala100=
ENST00000676426.1:c.299_300delinsCT	ENSP00000502359.1:p.Ala100=
ENST00000235329.9:c.299_300delinsCT	ENSP00000235329.5:p.Ala100=
ENST00000444836.5:c.299_300delinsCT	ENSP00000416338.1:p.Ala100=
NM_001127660.1:c.299_300delinsCT	NP_001121132.1:p.Ala100=
NM_014874.3:c.299_300delinsCT , LRG_255t1:c.299_300delinsCT	NP_055689.1:p.Ala100=
XM_005263543.2:c.299_300delinsCT	XP_005263600.1:p.Ala100=
XM_005263545.2:c.299_300delinsCT	XP_005263602.1:p.Ala100=
XM_005263547.2:c.299_300delinsCT	XP_005263604.1:p.Ala100=
XM_005263548.2:c.299_300delinsCT	XP_005263605.1:p.Ala100=
XM_005263543.3:c.299_300delinsCT	XP_005263600.1:p.Ala100=
XM_005263545.3:c.299_300delinsCT	XP_005263602.1:p.Ala100=
XM_005263547.3:c.299_300delinsCT	XP_005263604.1:p.Ala100=
XM_005263548.3:c.299_300delinsCT	XP_005263605.1:p.Ala100=
XM_024451299.1:c.299_300delinsCT	XP_024307067.1:p.Ala100=
NM_014874.4:c.299_300delinsCT MANE Select	NP_055689.1:p.Ala100=
NM_001127660.2:c.299_300delinsCT	NP_001121132.1:p.Ala100=