Canonical Allele Identifier: CA2742487707

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11992809_11992810insACA , CM000663.2:g.11992809_11992810insACA	GRCh38
NC_000001.10:g.12052866_12052867insACA , CM000663.1:g.12052866_12052867insACA	GRCh37
NC_000001.9:g.11975453_11975454insACA	NCBI36
NG_007945.1:g.17629_17630insACA , LRG_255:g.17629_17630insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.311+119_311+120insACA MANE Select	ENSP00000235329.5:n.311+119_311+120insACA
ENST00000674548.1:c.311+119_311+120insACA	ENSP00000502185.1:n.311+119_311+120insACA
ENST00000674658.1:c.-34-3347_-34-3346insACA	ENSP00000502334.1:n.-34-3347_-34-3346insACA
ENST00000674706.1:n.750+119_750+120insACA
ENST00000674817.1:c.311+119_311+120insACA	ENSP00000502151.1:n.311+119_311+120insACA
ENST00000674910.1:c.311+119_311+120insACA	ENSP00000501716.1:n.311+119_311+120insACA
ENST00000675053.1:c.311+119_311+120insACA	ENSP00000501646.1:n.311+119_311+120insACA
ENST00000675113.1:c.311+119_311+120insACA	ENSP00000502623.1:n.311+119_311+120insACA
ENST00000675194.1:n.736+119_736+120insACA
ENST00000675231.1:c.311+119_311+120insACA	ENSP00000502404.1:n.311+119_311+120insACA
ENST00000675298.1:c.311+119_311+120insACA	ENSP00000501839.1:n.311+119_311+120insACA
ENST00000675483.1:n.439+119_439+120insACA
ENST00000675512.1:c.*313+119_*313+120insACA	ENSP00000502630.1:n.*313+119_*313+120insACA
ENST00000675817.1:c.311+119_311+120insACA	ENSP00000502422.1:n.311+119_311+120insACA
ENST00000675872.1:n.562+119_562+120insACA
ENST00000675919.1:c.311+119_311+120insACA	ENSP00000501776.1:n.311+119_311+120insACA
ENST00000675959.1:n.708+119_708+120insACA
ENST00000675987.1:c.311+119_311+120insACA	ENSP00000502145.1:n.311+119_311+120insACA
ENST00000676293.1:c.311+119_311+120insACA	ENSP00000502362.1:n.311+119_311+120insACA
ENST00000676426.1:c.311+119_311+120insACA	ENSP00000502359.1:n.311+119_311+120insACA
ENST00000235329.9:c.311+119_311+120insACA	ENSP00000235329.5:n.311+119_311+120insACA
ENST00000444836.5:c.311+119_311+120insACA	ENSP00000416338.1:n.311+119_311+120insACA
NM_001127660.1:c.311+119_311+120insACA	NP_001121132.1:n.311+119_311+120insACA
NM_014874.3:c.311+119_311+120insACA , LRG_255t1:c.311+119_311+120insACA	NP_055689.1:n.311+119_311+120insACA
XM_005263543.2:c.311+119_311+120insACA	XP_005263600.1:n.311+119_311+120insACA
XM_005263545.2:c.311+119_311+120insACA	XP_005263602.1:n.311+119_311+120insACA
XM_005263547.2:c.311+119_311+120insACA	XP_005263604.1:n.311+119_311+120insACA
XM_005263548.2:c.311+119_311+120insACA	XP_005263605.1:n.311+119_311+120insACA
XM_005263543.3:c.311+119_311+120insACA	XP_005263600.1:n.311+119_311+120insACA
XM_005263545.3:c.311+119_311+120insACA	XP_005263602.1:n.311+119_311+120insACA
XM_005263547.3:c.311+119_311+120insACA	XP_005263604.1:n.311+119_311+120insACA
XM_005263548.3:c.311+119_311+120insACA	XP_005263605.1:n.311+119_311+120insACA
XM_024451299.1:c.311+119_311+120insACA	XP_024307067.1:n.311+119_311+120insACA
NM_014874.4:c.311+119_311+120insACA MANE Select	NP_055689.1:n.311+119_311+120insACA
NM_001127660.2:c.311+119_311+120insACA	NP_001121132.1:n.311+119_311+120insACA