Canonical Allele Identifier: CA1153896814

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980246G= , CM000663.2:g.11980246G=	GRCh38
NC_000001.10:g.12040303G= , CM000663.1:g.12040303G=	GRCh37
NC_000001.9:g.11962890G=	NCBI36
NG_007945.1:g.5066G= , LRG_255:g.5066G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-452G=	ENSP00000412023.1:n.-452G=
ENST00000674548.1:c.-333G=	ENSP00000502185.1:n.-333G=
ENST00000674817.1:c.-243G=	ENSP00000502151.1:n.-243G=
ENST00000675053.1:c.-291G=	ENSP00000501646.1:n.-291G=
ENST00000675194.1:n.38G=
ENST00000675298.1:c.-388G=	ENSP00000501839.1:n.-388G=
ENST00000675530.1:c.-384G=	ENSP00000501972.1:n.-384G=
ENST00000675817.1:c.-388G=	ENSP00000502422.1:n.-388G=
ENST00000675872.1:n.9G=
ENST00000675959.1:n.10G=
ENST00000676369.1:c.-456G=	ENSP00000502005.1:n.-456G=
ENST00000444836.5:c.-243G=	ENSP00000416338.1:n.-243G=
NM_001127660.1:c.-243G=	NP_001121132.1:n.-243G=
NM_014874.3:c.-388G= , LRG_255t1:c.-388G=	NP_055689.1:n.-388G=
XM_005263543.2:c.-456G=	XP_005263600.1:n.-456G=
XM_005263548.2:c.-452G=	XP_005263605.1:n.-452G=
XM_005263543.3:c.-456G=	XP_005263600.1:n.-456G=
XM_005263548.3:c.-452G=	XP_005263605.1:n.-452G=