Canonical Allele Identifier: CA1145870421

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980248G= , CM000663.2:g.11980248G=	GRCh38
NC_000001.10:g.12040305G= , CM000663.1:g.12040305G=	GRCh37
NC_000001.9:g.11962892G=	NCBI36
NG_007945.1:g.5068G= , LRG_255:g.5068G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-450G=	ENSP00000412023.1:n.-450G=
ENST00000674548.1:c.-331G=	ENSP00000502185.1:n.-331G=
ENST00000674817.1:c.-241G=	ENSP00000502151.1:n.-241G=
ENST00000675053.1:c.-289G=	ENSP00000501646.1:n.-289G=
ENST00000675194.1:n.40G=
ENST00000675298.1:c.-386G=	ENSP00000501839.1:n.-386G=
ENST00000675530.1:c.-382G=	ENSP00000501972.1:n.-382G=
ENST00000675817.1:c.-386G=	ENSP00000502422.1:n.-386G=
ENST00000675872.1:n.11G=
ENST00000675959.1:n.12G=
ENST00000676369.1:c.-454G=	ENSP00000502005.1:n.-454G=
ENST00000444836.5:c.-241G=	ENSP00000416338.1:n.-241G=
NM_001127660.1:c.-241G=	NP_001121132.1:n.-241G=
NM_014874.3:c.-386G= , LRG_255t1:c.-386G=	NP_055689.1:n.-386G=
XM_005263543.2:c.-454G=	XP_005263600.1:n.-454G=
XM_005263548.2:c.-450G=	XP_005263605.1:n.-450G=
XM_005263543.3:c.-454G=	XP_005263600.1:n.-454G=
XM_005263548.3:c.-450G=	XP_005263605.1:n.-450G=