Canonical Allele Identifier: CA2574216799

Gene: MFN2

Linked Data

• gnomAD v4: 1-12009752-G-GTTAGGGCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009753_12009761dup , CM000663.2:g.12009753_12009761dup	GRCh38
NC_000001.10:g.12069810_12069818dup , CM000663.1:g.12069810_12069818dup	GRCh37
NC_000001.9:g.11992397_11992405dup	NCBI36
NG_007945.1:g.34573_34581dup , LRG_255:g.34573_34581dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2204+27_2204+35dup MANE Select	ENSP00000235329.5:n.2204+27_2204+35dup
ENST00000674548.1:c.2204+27_2204+35dup	ENSP00000502185.1:n.2204+27_2204+35dup
ENST00000674658.1:c.1859+27_1859+35dup	ENSP00000502334.1:n.1859+27_1859+35dup
ENST00000674817.1:c.2204+27_2204+35dup	ENSP00000502151.1:n.2204+27_2204+35dup
ENST00000674910.1:c.2204+27_2204+35dup	ENSP00000501716.1:n.2204+27_2204+35dup
ENST00000675043.1:n.172+27_172+35dup
ENST00000675053.1:c.2204+27_2204+35dup	ENSP00000501646.1:n.2204+27_2204+35dup
ENST00000675113.1:c.2204+27_2204+35dup	ENSP00000502623.1:n.2204+27_2204+35dup
ENST00000675231.1:c.2204+27_2204+35dup	ENSP00000502404.1:n.2204+27_2204+35dup
ENST00000675298.1:c.2204+27_2204+35dup	ENSP00000501839.1:n.2204+27_2204+35dup
ENST00000675404.1:n.2439+27_2439+35dup
ENST00000675483.1:n.2332+27_2332+35dup
ENST00000675512.1:c.*2206+27_*2206+35dup	ENSP00000502630.1:n.*2206+27_*2206+35dup
ENST00000675528.1:n.1695+27_1695+35dup
ENST00000675817.1:c.2336+27_2336+35dup	ENSP00000502422.1:n.2336+27_2336+35dup
ENST00000675872.1:n.2564+27_2564+35dup
ENST00000675919.1:c.2204+27_2204+35dup	ENSP00000501776.1:n.2204+27_2204+35dup
ENST00000675959.1:n.2710+27_2710+35dup
ENST00000675987.1:c.*177+27_*177+35dup	ENSP00000502145.1:n.*177+27_*177+35dup
ENST00000676293.1:c.2204+27_2204+35dup	ENSP00000502362.1:n.2204+27_2204+35dup
ENST00000676295.1:n.617+27_617+35dup
ENST00000676426.1:c.*1204+27_*1204+35dup	ENSP00000502359.1:n.*1204+27_*1204+35dup
ENST00000235329.9:c.2204+27_2204+35dup	ENSP00000235329.5:n.2204+27_2204+35dup
ENST00000444836.5:c.2204+27_2204+35dup	ENSP00000416338.1:n.2204+27_2204+35dup
NM_001127660.1:c.2204+27_2204+35dup	NP_001121132.1:n.2204+27_2204+35dup
NM_014874.3:c.2204+27_2204+35dup , LRG_255t1:c.2204+27_2204+35dup	NP_055689.1:n.2204+27_2204+35dup
XM_005263543.2:c.2204+27_2204+35dup	XP_005263600.1:n.2204+27_2204+35dup
XM_005263545.2:c.2204+27_2204+35dup	XP_005263602.1:n.2204+27_2204+35dup
XM_005263547.2:c.2204+27_2204+35dup	XP_005263604.1:n.2204+27_2204+35dup
XM_005263548.2:c.2204+27_2204+35dup	XP_005263605.1:n.2204+27_2204+35dup
XM_005263543.3:c.2204+27_2204+35dup	XP_005263600.1:n.2204+27_2204+35dup
XM_005263545.3:c.2204+27_2204+35dup	XP_005263602.1:n.2204+27_2204+35dup
XM_005263547.3:c.2204+27_2204+35dup	XP_005263604.1:n.2204+27_2204+35dup
XM_005263548.3:c.2204+27_2204+35dup	XP_005263605.1:n.2204+27_2204+35dup
XM_024451299.1:c.2204+27_2204+35dup	XP_024307067.1:n.2204+27_2204+35dup
NM_014874.4:c.2204+27_2204+35dup MANE Select	NP_055689.1:n.2204+27_2204+35dup
NM_001127660.2:c.2204+27_2204+35dup	NP_001121132.1:n.2204+27_2204+35dup