Canonical Allele Identifier: CA1139922329

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980267A= , CM000663.2:g.11980267A=	GRCh38
NC_000001.10:g.12040324A= , CM000663.1:g.12040324A=	GRCh37
NC_000001.9:g.11962911A=	NCBI36
NG_007945.1:g.5087A= , LRG_255:g.5087A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-431A=	ENSP00000412023.1:n.-431A=
ENST00000674548.1:c.-312A=	ENSP00000502185.1:n.-312A=
ENST00000674706.1:n.9A=
ENST00000674817.1:c.-222A=	ENSP00000502151.1:n.-222A=
ENST00000675053.1:c.-270A=	ENSP00000501646.1:n.-270A=
ENST00000675194.1:n.59A=
ENST00000675298.1:c.-367A=	ENSP00000501839.1:n.-367A=
ENST00000675530.1:c.-363A=	ENSP00000501972.1:n.-363A=
ENST00000675817.1:c.-367A=	ENSP00000502422.1:n.-367A=
ENST00000675872.1:n.30A=
ENST00000675959.1:n.31A=
ENST00000676369.1:c.-435A=	ENSP00000502005.1:n.-435A=
ENST00000676426.1:c.-367A=	ENSP00000502359.1:n.-367A=
ENST00000444836.5:c.-222A=	ENSP00000416338.1:n.-222A=
NM_001127660.1:c.-222A=	NP_001121132.1:n.-222A=
NM_014874.3:c.-367A= , LRG_255t1:c.-367A=	NP_055689.1:n.-367A=
XM_005263543.2:c.-435A=	XP_005263600.1:n.-435A=
XM_005263548.2:c.-431A=	XP_005263605.1:n.-431A=
XM_005263543.3:c.-435A=	XP_005263600.1:n.-435A=
XM_005263548.3:c.-431A=	XP_005263605.1:n.-431A=