Canonical Allele Identifier: CA2742488434

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12002222_12002223insC , CM000663.2:g.12002222_12002223insC	GRCh38
NC_000001.10:g.12062279_12062280insC , CM000663.1:g.12062279_12062280insC	GRCh37
NC_000001.9:g.11984866_11984867insC	NCBI36
NG_007945.1:g.27042_27043insC , LRG_255:g.27042_27043insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.1160+119_1160+120insC MANE Select	ENSP00000235329.5:n.1160+119_1160+120insC
ENST00000674548.1:c.1160+119_1160+120insC	ENSP00000502185.1:n.1160+119_1160+120insC
ENST00000674658.1:c.815+119_815+120insC	ENSP00000502334.1:n.815+119_815+120insC
ENST00000674817.1:c.1160+119_1160+120insC	ENSP00000502151.1:n.1160+119_1160+120insC
ENST00000674910.1:c.1160+119_1160+120insC	ENSP00000501716.1:n.1160+119_1160+120insC
ENST00000675053.1:c.1160+119_1160+120insC	ENSP00000501646.1:n.1160+119_1160+120insC
ENST00000675113.1:c.1160+119_1160+120insC	ENSP00000502623.1:n.1160+119_1160+120insC
ENST00000675194.1:n.1704_1705insC
ENST00000675231.1:c.1160+119_1160+120insC	ENSP00000502404.1:n.1160+119_1160+120insC
ENST00000675298.1:c.1160+119_1160+120insC	ENSP00000501839.1:n.1160+119_1160+120insC
ENST00000675404.1:n.1395+119_1395+120insC
ENST00000675483.1:n.1288+119_1288+120insC
ENST00000675512.1:c.*1162+119_*1162+120insC	ENSP00000502630.1:n.*1162+119_*1162+120insC
ENST00000675528.1:n.651+119_651+120insC
ENST00000675817.1:c.1160+119_1160+120insC	ENSP00000502422.1:n.1160+119_1160+120insC
ENST00000675872.1:n.1520+119_1520+120insC
ENST00000675919.1:c.1160+119_1160+120insC	ENSP00000501776.1:n.1160+119_1160+120insC
ENST00000675959.1:n.1666+119_1666+120insC
ENST00000675987.1:c.1160+119_1160+120insC	ENSP00000502145.1:n.1160+119_1160+120insC
ENST00000676293.1:c.1160+119_1160+120insC	ENSP00000502362.1:n.1160+119_1160+120insC
ENST00000676426.1:c.*160+119_*160+120insC	ENSP00000502359.1:n.*160+119_*160+120insC
ENST00000235329.9:c.1160+119_1160+120insC	ENSP00000235329.5:n.1160+119_1160+120insC
ENST00000444836.5:c.1160+119_1160+120insC	ENSP00000416338.1:n.1160+119_1160+120insC
NM_001127660.1:c.1160+119_1160+120insC	NP_001121132.1:n.1160+119_1160+120insC
NM_014874.3:c.1160+119_1160+120insC , LRG_255t1:c.1160+119_1160+120insC	NP_055689.1:n.1160+119_1160+120insC
XM_005263543.2:c.1160+119_1160+120insC	XP_005263600.1:n.1160+119_1160+120insC
XM_005263545.2:c.1160+119_1160+120insC	XP_005263602.1:n.1160+119_1160+120insC
XM_005263547.2:c.1160+119_1160+120insC	XP_005263604.1:n.1160+119_1160+120insC
XM_005263548.2:c.1160+119_1160+120insC	XP_005263605.1:n.1160+119_1160+120insC
XM_005263543.3:c.1160+119_1160+120insC	XP_005263600.1:n.1160+119_1160+120insC
XM_005263545.3:c.1160+119_1160+120insC	XP_005263602.1:n.1160+119_1160+120insC
XM_005263547.3:c.1160+119_1160+120insC	XP_005263604.1:n.1160+119_1160+120insC
XM_005263548.3:c.1160+119_1160+120insC	XP_005263605.1:n.1160+119_1160+120insC
XM_024451299.1:c.1160+119_1160+120insC	XP_024307067.1:n.1160+119_1160+120insC
NM_014874.4:c.1160+119_1160+120insC MANE Select	NP_055689.1:n.1160+119_1160+120insC
NM_001127660.2:c.1160+119_1160+120insC	NP_001121132.1:n.1160+119_1160+120insC