Canonical Allele Identifier: CA2742489510

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009873_12009878del , CM000663.2:g.12009873_12009878del	GRCh38
NC_000001.10:g.12069930_12069935del , CM000663.1:g.12069930_12069935del	GRCh37
NC_000001.9:g.11992517_11992522del	NCBI36
NG_007945.1:g.34693_34698del , LRG_255:g.34693_34698del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2204+147_2204+152del MANE Select	ENSP00000235329.5:n.2204+147_2204+152del
ENST00000674548.1:c.2204+147_2204+152del	ENSP00000502185.1:n.2204+147_2204+152del
ENST00000674658.1:c.1859+147_1859+152del	ENSP00000502334.1:n.1859+147_1859+152del
ENST00000674817.1:c.2204+147_2204+152del	ENSP00000502151.1:n.2204+147_2204+152del
ENST00000674910.1:c.2204+147_2204+152del	ENSP00000501716.1:n.2204+147_2204+152del
ENST00000675043.1:n.172+147_172+152del
ENST00000675053.1:c.2204+147_2204+152del	ENSP00000501646.1:n.2204+147_2204+152del
ENST00000675113.1:c.2204+147_2204+152del	ENSP00000502623.1:n.2204+147_2204+152del
ENST00000675231.1:c.2204+147_2204+152del	ENSP00000502404.1:n.2204+147_2204+152del
ENST00000675298.1:c.2204+147_2204+152del	ENSP00000501839.1:n.2204+147_2204+152del
ENST00000675404.1:n.2439+147_2439+152del
ENST00000675483.1:n.2332+147_2332+152del
ENST00000675512.1:c.*2206+147_*2206+152del	ENSP00000502630.1:n.*2206+147_*2206+152del
ENST00000675528.1:n.1695+147_1695+152del
ENST00000675817.1:c.2336+147_2336+152del	ENSP00000502422.1:n.2336+147_2336+152del
ENST00000675872.1:n.2564+147_2564+152del
ENST00000675919.1:c.2204+147_2204+152del	ENSP00000501776.1:n.2204+147_2204+152del
ENST00000675959.1:n.2710+147_2710+152del
ENST00000675987.1:c.*177+147_*177+152del	ENSP00000502145.1:n.*177+147_*177+152del
ENST00000676293.1:c.2204+147_2204+152del	ENSP00000502362.1:n.2204+147_2204+152del
ENST00000676295.1:n.617+147_617+152del
ENST00000676426.1:c.*1204+147_*1204+152del	ENSP00000502359.1:n.*1204+147_*1204+152del
ENST00000235329.9:c.2204+147_2204+152del	ENSP00000235329.5:n.2204+147_2204+152del
ENST00000444836.5:c.2204+147_2204+152del	ENSP00000416338.1:n.2204+147_2204+152del
NM_001127660.1:c.2204+147_2204+152del	NP_001121132.1:n.2204+147_2204+152del
NM_014874.3:c.2204+147_2204+152del , LRG_255t1:c.2204+147_2204+152del	NP_055689.1:n.2204+147_2204+152del
XM_005263543.2:c.2204+147_2204+152del	XP_005263600.1:n.2204+147_2204+152del
XM_005263545.2:c.2204+147_2204+152del	XP_005263602.1:n.2204+147_2204+152del
XM_005263547.2:c.2204+147_2204+152del	XP_005263604.1:n.2204+147_2204+152del
XM_005263548.2:c.2204+147_2204+152del	XP_005263605.1:n.2204+147_2204+152del
XM_005263543.3:c.2204+147_2204+152del	XP_005263600.1:n.2204+147_2204+152del
XM_005263545.3:c.2204+147_2204+152del	XP_005263602.1:n.2204+147_2204+152del
XM_005263547.3:c.2204+147_2204+152del	XP_005263604.1:n.2204+147_2204+152del
XM_005263548.3:c.2204+147_2204+152del	XP_005263605.1:n.2204+147_2204+152del
XM_024451299.1:c.2204+147_2204+152del	XP_024307067.1:n.2204+147_2204+152del
NM_014874.4:c.2204+147_2204+152del MANE Select	NP_055689.1:n.2204+147_2204+152del
NM_001127660.2:c.2204+147_2204+152del	NP_001121132.1:n.2204+147_2204+152del