Canonical Allele Identifier: CA2742489190

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12006790_12007015del , CM000663.2:g.12006790_12007015del	GRCh38
NC_000001.10:g.12066847_12067072del , CM000663.1:g.12066847_12067072del	GRCh37
NC_000001.9:g.11989434_11989659del	NCBI36
NG_007945.1:g.31610_31835del , LRG_255:g.31610_31835del

Transcript Alleles

HGVS	Amino-acid change
ENST00000235329.10:c.1872+97_1873-38del MANE Select	ENSP00000235329.5:n.1872+97_1873-38del
ENST00000674548.1:c.1872+97_1873-38del	ENSP00000502185.1:n.1872+97_1873-38del
ENST00000674658.1:c.1527+97_1528-38del	ENSP00000502334.1:n.1527+97_1528-38del
ENST00000674817.1:c.1872+97_1873-38del	ENSP00000502151.1:n.1872+97_1873-38del
ENST00000674910.1:c.1872+97_1873-38del	ENSP00000501716.1:n.1872+97_1873-38del
ENST00000675053.1:c.1872+97_1873-38del	ENSP00000501646.1:n.1872+97_1873-38del
ENST00000675113.1:c.1872+97_1873-38del	ENSP00000502623.1:n.1872+97_1873-38del
ENST00000675231.1:c.1872+97_1873-38del	ENSP00000502404.1:n.1872+97_1873-38del
ENST00000675298.1:c.1872+97_1873-38del	ENSP00000501839.1:n.1872+97_1873-38del
ENST00000675404.1:n.2107+97_2108-38del
ENST00000675483.1:n.2000+97_2001-38del
ENST00000675512.1:c.*1874+97_*1875-38del	ENSP00000502630.1:n.*1874+97_*1875-38del
ENST00000675528.1:n.1363+97_1364-38del
ENST00000675817.1:c.2004+97_2005-38del	ENSP00000502422.1:n.2004+97_2005-38del
ENST00000675872.1:n.2232+97_2233-38del
ENST00000675919.1:c.1872+97_1873-38del	ENSP00000501776.1:n.1872+97_1873-38del
ENST00000675959.1:n.2378+97_2379-38del
ENST00000675987.1:c.1872+97_1873-38del	ENSP00000502145.1:n.1872+97_1873-38del
ENST00000676293.1:c.1872+97_1873-38del	ENSP00000502362.1:n.1872+97_1873-38del
ENST00000676295.1:n.23_248del
ENST00000676426.1:c.*872+97_*873-38del	ENSP00000502359.1:n.*872+97_*873-38del
ENST00000235329.9:c.1872+97_1873-38del	ENSP00000235329.5:n.1872+97_1873-38del
ENST00000444836.5:c.1872+97_1873-38del	ENSP00000416338.1:n.1872+97_1873-38del
NM_001127660.1:c.1872+97_1873-38del	NP_001121132.1:n.1872+97_1873-38del
NM_014874.3:c.1872+97_1873-38del , LRG_255t1:c.1872+97_1873-38del	NP_055689.1:n.1872+97_1873-38del
XM_005263543.2:c.1872+97_1873-38del	XP_005263600.1:n.1872+97_1873-38del
XM_005263545.2:c.1872+97_1873-38del	XP_005263602.1:n.1872+97_1873-38del
XM_005263547.2:c.1872+97_1873-38del	XP_005263604.1:n.1872+97_1873-38del
XM_005263548.2:c.1872+97_1873-38del	XP_005263605.1:n.1872+97_1873-38del
XM_005263543.3:c.1872+97_1873-38del	XP_005263600.1:n.1872+97_1873-38del
XM_005263545.3:c.1872+97_1873-38del	XP_005263602.1:n.1872+97_1873-38del
XM_005263547.3:c.1872+97_1873-38del	XP_005263604.1:n.1872+97_1873-38del
XM_005263548.3:c.1872+97_1873-38del	XP_005263605.1:n.1872+97_1873-38del
XM_024451299.1:c.1872+97_1873-38del	XP_024307067.1:n.1872+97_1873-38del
NM_014874.4:c.1872+97_1873-38del MANE Select	NP_055689.1:n.1872+97_1873-38del
NM_001127660.2:c.1872+97_1873-38del	NP_001121132.1:n.1872+97_1873-38del