Canonical Allele Identifier: CA1147653669

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980376G= , CM000663.2:g.11980376G=	GRCh38
NC_000001.10:g.12040433G= , CM000663.1:g.12040433G=	GRCh37
NC_000001.9:g.11963020G=	NCBI36
NG_007945.1:g.5196G= , LRG_255:g.5196G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-322G=	ENSP00000412023.1:n.-322G=
ENST00000674548.1:c.-203G=	ENSP00000502185.1:n.-203G=
ENST00000674658.1:c.-356G=	ENSP00000502334.1:n.-356G=
ENST00000674706.1:n.118G=
ENST00000674817.1:c.-113G=	ENSP00000502151.1:n.-113G=
ENST00000674910.1:c.-235G=	ENSP00000501716.1:n.-235G=
ENST00000675053.1:c.-161G=	ENSP00000501646.1:n.-161G=
ENST00000675194.1:n.168G=
ENST00000675231.1:c.-486G=	ENSP00000502404.1:n.-486G=
ENST00000675298.1:c.-258G=	ENSP00000501839.1:n.-258G=
ENST00000675530.1:c.-254G=	ENSP00000501972.1:n.-254G=
ENST00000675817.1:c.-258G=	ENSP00000502422.1:n.-258G=
ENST00000675872.1:n.139G=
ENST00000675959.1:n.140G=
ENST00000676369.1:c.-326G=	ENSP00000502005.1:n.-326G=
ENST00000676426.1:c.-258G=	ENSP00000502359.1:n.-258G=
ENST00000235329.9:c.-258G=	ENSP00000235329.5:n.-258G=
ENST00000444836.5:c.-113G=	ENSP00000416338.1:n.-113G=
ENST00000484391.5:n.7G=
ENST00000490079.5:n.78G=
NM_001127660.1:c.-113G=	NP_001121132.1:n.-113G=
NM_014874.3:c.-258G= , LRG_255t1:c.-258G=	NP_055689.1:n.-258G=
XM_005263543.2:c.-326G=	XP_005263600.1:n.-326G=
XM_005263545.2:c.-254G=	XP_005263602.1:n.-254G=
XM_005263548.2:c.-322G=	XP_005263605.1:n.-322G=
XM_005263543.3:c.-326G=	XP_005263600.1:n.-326G=
XM_005263545.3:c.-254G=	XP_005263602.1:n.-254G=
XM_005263548.3:c.-322G=	XP_005263605.1:n.-322G=
XM_024451299.1:c.-486G=	XP_024307067.1:n.-486G=