Canonical Allele Identifier: CA1153926968

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009274_12009276delinsCTG , CM000663.2:g.12009274_12009276delinsCTG	GRCh38
NC_000001.10:g.12069331_12069333delinsCTG , CM000663.1:g.12069331_12069333delinsCTG	GRCh37
NC_000001.9:g.11991918_11991920delinsCTG	NCBI36
NG_007945.1:g.34094_34096delinsCTG , LRG_255:g.34094_34096delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2070-318_2070-316delinsCTG MANE Select	ENSP00000235329.5:n.2070-318_2070-316delinsCTG
ENST00000674548.1:c.2070-318_2070-316delinsCTG	ENSP00000502185.1:n.2070-318_2070-316delinsCTG
ENST00000674658.1:c.1725-318_1725-316delinsCTG	ENSP00000502334.1:n.1725-318_1725-316delinsCTG
ENST00000674817.1:c.2070-318_2070-316delinsCTG	ENSP00000502151.1:n.2070-318_2070-316delinsCTG
ENST00000674910.1:c.2070-318_2070-316delinsCTG	ENSP00000501716.1:n.2070-318_2070-316delinsCTG
ENST00000675053.1:c.2070-318_2070-316delinsCTG	ENSP00000501646.1:n.2070-318_2070-316delinsCTG
ENST00000675113.1:c.2070-318_2070-316delinsCTG	ENSP00000502623.1:n.2070-318_2070-316delinsCTG
ENST00000675231.1:c.2070-318_2070-316delinsCTG	ENSP00000502404.1:n.2070-318_2070-316delinsCTG
ENST00000675298.1:c.2070-318_2070-316delinsCTG	ENSP00000501839.1:n.2070-318_2070-316delinsCTG
ENST00000675404.1:n.2305-318_2305-316delinsCTG
ENST00000675483.1:n.2198-318_2198-316delinsCTG
ENST00000675512.1:c.*2072-318_*2072-316delinsCTG	ENSP00000502630.1:n.*2072-318_*2072-316delinsCTG
ENST00000675528.1:n.1561-318_1561-316delinsCTG
ENST00000675817.1:c.2202-318_2202-316delinsCTG	ENSP00000502422.1:n.2202-318_2202-316delinsCTG
ENST00000675872.1:n.2430-318_2430-316delinsCTG
ENST00000675919.1:c.2070-318_2070-316delinsCTG	ENSP00000501776.1:n.2070-318_2070-316delinsCTG
ENST00000675959.1:n.2576-318_2576-316delinsCTG
ENST00000675987.1:c.*43-318_*43-316delinsCTG	ENSP00000502145.1:n.*43-318_*43-316delinsCTG
ENST00000676293.1:c.2070-318_2070-316delinsCTG	ENSP00000502362.1:n.2070-318_2070-316delinsCTG
ENST00000676295.1:n.483-318_483-316delinsCTG
ENST00000676426.1:c.*1070-318_*1070-316delinsCTG	ENSP00000502359.1:n.*1070-318_*1070-316delinsCTG
ENST00000235329.9:c.2070-318_2070-316delinsCTG	ENSP00000235329.5:n.2070-318_2070-316delinsCTG
ENST00000444836.5:c.2070-318_2070-316delinsCTG	ENSP00000416338.1:n.2070-318_2070-316delinsCTG
NM_001127660.1:c.2070-318_2070-316delinsCTG	NP_001121132.1:n.2070-318_2070-316delinsCTG
NM_014874.3:c.2070-318_2070-316delinsCTG , LRG_255t1:c.2070-318_2070-316delinsCTG	NP_055689.1:n.2070-318_2070-316delinsCTG
XM_005263543.2:c.2070-318_2070-316delinsCTG	XP_005263600.1:n.2070-318_2070-316delinsCTG
XM_005263545.2:c.2070-318_2070-316delinsCTG	XP_005263602.1:n.2070-318_2070-316delinsCTG
XM_005263547.2:c.2070-318_2070-316delinsCTG	XP_005263604.1:n.2070-318_2070-316delinsCTG
XM_005263548.2:c.2070-318_2070-316delinsCTG	XP_005263605.1:n.2070-318_2070-316delinsCTG
XM_005263543.3:c.2070-318_2070-316delinsCTG	XP_005263600.1:n.2070-318_2070-316delinsCTG
XM_005263545.3:c.2070-318_2070-316delinsCTG	XP_005263602.1:n.2070-318_2070-316delinsCTG
XM_005263547.3:c.2070-318_2070-316delinsCTG	XP_005263604.1:n.2070-318_2070-316delinsCTG
XM_005263548.3:c.2070-318_2070-316delinsCTG	XP_005263605.1:n.2070-318_2070-316delinsCTG
XM_024451299.1:c.2070-318_2070-316delinsCTG	XP_024307067.1:n.2070-318_2070-316delinsCTG
NM_014874.4:c.2070-318_2070-316delinsCTG MANE Select	NP_055689.1:n.2070-318_2070-316delinsCTG
NM_001127660.2:c.2070-318_2070-316delinsCTG	NP_001121132.1:n.2070-318_2070-316delinsCTG