Canonical Allele Identifier: CA2643323018

Gene: MFN2

Linked Data

• gnomAD v4: 1-12009584-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009584_12009585insG , CM000663.2:g.12009584_12009585insG	GRCh38
NC_000001.10:g.12069641_12069642insG , CM000663.1:g.12069641_12069642insG	GRCh37
NC_000001.9:g.11992228_11992229insG	NCBI36
NG_007945.1:g.34404_34405insG , LRG_255:g.34404_34405insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000235329.10:c.2070-8_2070-7insG MANE Select	ENSP00000235329.5:n.2070-8_2070-7insG
ENST00000674548.1:c.2070-8_2070-7insG	ENSP00000502185.1:n.2070-8_2070-7insG
ENST00000674658.1:c.1725-8_1725-7insG	ENSP00000502334.1:n.1725-8_1725-7insG
ENST00000674817.1:c.2070-8_2070-7insG	ENSP00000502151.1:n.2070-8_2070-7insG
ENST00000674910.1:c.2070-8_2070-7insG	ENSP00000501716.1:n.2070-8_2070-7insG
ENST00000675043.1:n.30_31insG
ENST00000675053.1:c.2070-8_2070-7insG	ENSP00000501646.1:n.2070-8_2070-7insG
ENST00000675113.1:c.2070-8_2070-7insG	ENSP00000502623.1:n.2070-8_2070-7insG
ENST00000675231.1:c.2070-8_2070-7insG	ENSP00000502404.1:n.2070-8_2070-7insG
ENST00000675298.1:c.2070-8_2070-7insG	ENSP00000501839.1:n.2070-8_2070-7insG
ENST00000675404.1:n.2305-8_2305-7insG
ENST00000675483.1:n.2198-8_2198-7insG
ENST00000675512.1:c.*2072-8_*2072-7insG	ENSP00000502630.1:n.*2072-8_*2072-7insG
ENST00000675528.1:n.1561-8_1561-7insG
ENST00000675817.1:c.2202-8_2202-7insG	ENSP00000502422.1:n.2202-8_2202-7insG
ENST00000675872.1:n.2430-8_2430-7insG
ENST00000675919.1:c.2070-8_2070-7insG	ENSP00000501776.1:n.2070-8_2070-7insG
ENST00000675959.1:n.2576-8_2576-7insG
ENST00000675987.1:c.*43-8_*43-7insG	ENSP00000502145.1:n.*43-8_*43-7insG
ENST00000676293.1:c.2070-8_2070-7insG	ENSP00000502362.1:n.2070-8_2070-7insG
ENST00000676295.1:n.483-8_483-7insG
ENST00000676426.1:c.*1070-8_*1070-7insG	ENSP00000502359.1:n.*1070-8_*1070-7insG
ENST00000235329.9:c.2070-8_2070-7insG	ENSP00000235329.5:n.2070-8_2070-7insG
ENST00000444836.5:c.2070-8_2070-7insG	ENSP00000416338.1:n.2070-8_2070-7insG
NM_001127660.1:c.2070-8_2070-7insG	NP_001121132.1:n.2070-8_2070-7insG
NM_014874.3:c.2070-8_2070-7insG , LRG_255t1:c.2070-8_2070-7insG	NP_055689.1:n.2070-8_2070-7insG
XM_005263543.2:c.2070-8_2070-7insG	XP_005263600.1:n.2070-8_2070-7insG
XM_005263545.2:c.2070-8_2070-7insG	XP_005263602.1:n.2070-8_2070-7insG
XM_005263547.2:c.2070-8_2070-7insG	XP_005263604.1:n.2070-8_2070-7insG
XM_005263548.2:c.2070-8_2070-7insG	XP_005263605.1:n.2070-8_2070-7insG
XM_005263543.3:c.2070-8_2070-7insG	XP_005263600.1:n.2070-8_2070-7insG
XM_005263545.3:c.2070-8_2070-7insG	XP_005263602.1:n.2070-8_2070-7insG
XM_005263547.3:c.2070-8_2070-7insG	XP_005263604.1:n.2070-8_2070-7insG
XM_005263548.3:c.2070-8_2070-7insG	XP_005263605.1:n.2070-8_2070-7insG
XM_024451299.1:c.2070-8_2070-7insG	XP_024307067.1:n.2070-8_2070-7insG
NM_014874.4:c.2070-8_2070-7insG MANE Select	NP_055689.1:n.2070-8_2070-7insG
NM_001127660.2:c.2070-8_2070-7insG	NP_001121132.1:n.2070-8_2070-7insG