Canonical Allele Identifier: CA2742487816

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11992824_11992841del , CM000663.2:g.11992824_11992841del	GRCh38
NC_000001.10:g.12052881_12052898del , CM000663.1:g.12052881_12052898del	GRCh37
NC_000001.9:g.11975468_11975485del	NCBI36
NG_007945.1:g.17644_17661del , LRG_255:g.17644_17661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.311+134_311+151del MANE Select	ENSP00000235329.5:n.311+134_311+151del
ENST00000674548.1:c.311+134_311+151del	ENSP00000502185.1:n.311+134_311+151del
ENST00000674658.1:c.-34-3332_-34-3315del	ENSP00000502334.1:n.-34-3332_-34-3315del
ENST00000674706.1:n.750+134_750+151del
ENST00000674817.1:c.311+134_311+151del	ENSP00000502151.1:n.311+134_311+151del
ENST00000674910.1:c.311+134_311+151del	ENSP00000501716.1:n.311+134_311+151del
ENST00000675053.1:c.311+134_311+151del	ENSP00000501646.1:n.311+134_311+151del
ENST00000675113.1:c.311+134_311+151del	ENSP00000502623.1:n.311+134_311+151del
ENST00000675194.1:n.736+134_736+151del
ENST00000675231.1:c.311+134_311+151del	ENSP00000502404.1:n.311+134_311+151del
ENST00000675298.1:c.311+134_311+151del	ENSP00000501839.1:n.311+134_311+151del
ENST00000675483.1:n.439+134_439+151del
ENST00000675512.1:c.*313+134_*313+151del	ENSP00000502630.1:n.*313+134_*313+151del
ENST00000675817.1:c.311+134_311+151del	ENSP00000502422.1:n.311+134_311+151del
ENST00000675872.1:n.562+134_562+151del
ENST00000675919.1:c.311+134_311+151del	ENSP00000501776.1:n.311+134_311+151del
ENST00000675959.1:n.708+134_708+151del
ENST00000675987.1:c.311+134_311+151del	ENSP00000502145.1:n.311+134_311+151del
ENST00000676293.1:c.311+134_311+151del	ENSP00000502362.1:n.311+134_311+151del
ENST00000676426.1:c.311+134_311+151del	ENSP00000502359.1:n.311+134_311+151del
ENST00000235329.9:c.311+134_311+151del	ENSP00000235329.5:n.311+134_311+151del
ENST00000444836.5:c.311+134_311+151del	ENSP00000416338.1:n.311+134_311+151del
NM_001127660.1:c.311+134_311+151del	NP_001121132.1:n.311+134_311+151del
NM_014874.3:c.311+134_311+151del , LRG_255t1:c.311+134_311+151del	NP_055689.1:n.311+134_311+151del
XM_005263543.2:c.311+134_311+151del	XP_005263600.1:n.311+134_311+151del
XM_005263545.2:c.311+134_311+151del	XP_005263602.1:n.311+134_311+151del
XM_005263547.2:c.311+134_311+151del	XP_005263604.1:n.311+134_311+151del
XM_005263548.2:c.311+134_311+151del	XP_005263605.1:n.311+134_311+151del
XM_005263543.3:c.311+134_311+151del	XP_005263600.1:n.311+134_311+151del
XM_005263545.3:c.311+134_311+151del	XP_005263602.1:n.311+134_311+151del
XM_005263547.3:c.311+134_311+151del	XP_005263604.1:n.311+134_311+151del
XM_005263548.3:c.311+134_311+151del	XP_005263605.1:n.311+134_311+151del
XM_024451299.1:c.311+134_311+151del	XP_024307067.1:n.311+134_311+151del
NM_014874.4:c.311+134_311+151del MANE Select	NP_055689.1:n.311+134_311+151del
NM_001127660.2:c.311+134_311+151del	NP_001121132.1:n.311+134_311+151del