Canonical Allele Identifier: CA2742489598

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009927_12009928del , CM000663.2:g.12009927_12009928del	GRCh38
NC_000001.10:g.12069984_12069985del , CM000663.1:g.12069984_12069985del	GRCh37
NC_000001.9:g.11992571_11992572del	NCBI36
NG_007945.1:g.34747_34748del , LRG_255:g.34747_34748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2204+201_2204+202del MANE Select	ENSP00000235329.5:n.2204+201_2204+202del
ENST00000674548.1:c.2204+201_2204+202del	ENSP00000502185.1:n.2204+201_2204+202del
ENST00000674658.1:c.1859+201_1859+202del	ENSP00000502334.1:n.1859+201_1859+202del
ENST00000674817.1:c.2204+201_2204+202del	ENSP00000502151.1:n.2204+201_2204+202del
ENST00000674910.1:c.2204+201_2204+202del	ENSP00000501716.1:n.2204+201_2204+202del
ENST00000675043.1:n.172+201_172+202del
ENST00000675053.1:c.2204+201_2204+202del	ENSP00000501646.1:n.2204+201_2204+202del
ENST00000675113.1:c.2204+201_2204+202del	ENSP00000502623.1:n.2204+201_2204+202del
ENST00000675231.1:c.2204+201_2204+202del	ENSP00000502404.1:n.2204+201_2204+202del
ENST00000675298.1:c.2204+201_2204+202del	ENSP00000501839.1:n.2204+201_2204+202del
ENST00000675404.1:n.2439+201_2439+202del
ENST00000675483.1:n.2332+201_2332+202del
ENST00000675512.1:c.*2206+201_*2206+202del	ENSP00000502630.1:n.*2206+201_*2206+202del
ENST00000675528.1:n.1695+201_1695+202del
ENST00000675817.1:c.2336+201_2336+202del	ENSP00000502422.1:n.2336+201_2336+202del
ENST00000675872.1:n.2564+201_2564+202del
ENST00000675919.1:c.2204+201_2204+202del	ENSP00000501776.1:n.2204+201_2204+202del
ENST00000675959.1:n.2710+201_2710+202del
ENST00000675987.1:c.*177+201_*177+202del	ENSP00000502145.1:n.*177+201_*177+202del
ENST00000676293.1:c.2204+201_2204+202del	ENSP00000502362.1:n.2204+201_2204+202del
ENST00000676295.1:n.617+201_617+202del
ENST00000676426.1:c.*1204+201_*1204+202del	ENSP00000502359.1:n.*1204+201_*1204+202del
ENST00000235329.9:c.2204+201_2204+202del	ENSP00000235329.5:n.2204+201_2204+202del
ENST00000444836.5:c.2204+201_2204+202del	ENSP00000416338.1:n.2204+201_2204+202del
NM_001127660.1:c.2204+201_2204+202del	NP_001121132.1:n.2204+201_2204+202del
NM_014874.3:c.2204+201_2204+202del , LRG_255t1:c.2204+201_2204+202del	NP_055689.1:n.2204+201_2204+202del
XM_005263543.2:c.2204+201_2204+202del	XP_005263600.1:n.2204+201_2204+202del
XM_005263545.2:c.2204+201_2204+202del	XP_005263602.1:n.2204+201_2204+202del
XM_005263547.2:c.2204+201_2204+202del	XP_005263604.1:n.2204+201_2204+202del
XM_005263548.2:c.2204+201_2204+202del	XP_005263605.1:n.2204+201_2204+202del
XM_005263543.3:c.2204+201_2204+202del	XP_005263600.1:n.2204+201_2204+202del
XM_005263545.3:c.2204+201_2204+202del	XP_005263602.1:n.2204+201_2204+202del
XM_005263547.3:c.2204+201_2204+202del	XP_005263604.1:n.2204+201_2204+202del
XM_005263548.3:c.2204+201_2204+202del	XP_005263605.1:n.2204+201_2204+202del
XM_024451299.1:c.2204+201_2204+202del	XP_024307067.1:n.2204+201_2204+202del
NM_014874.4:c.2204+201_2204+202del MANE Select	NP_055689.1:n.2204+201_2204+202del
NM_001127660.2:c.2204+201_2204+202del	NP_001121132.1:n.2204+201_2204+202del