Canonical Allele Identifier: CA1153896840

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980277A= , CM000663.2:g.11980277A=	GRCh38
NC_000001.10:g.12040334A= , CM000663.1:g.12040334A=	GRCh37
NC_000001.9:g.11962921A=	NCBI36
NG_007945.1:g.5097A= , LRG_255:g.5097A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-421A=	ENSP00000412023.1:n.-421A=
ENST00000674548.1:c.-302A=	ENSP00000502185.1:n.-302A=
ENST00000674658.1:c.-455A=	ENSP00000502334.1:n.-455A=
ENST00000674706.1:n.19A=
ENST00000674817.1:c.-212A=	ENSP00000502151.1:n.-212A=
ENST00000675053.1:c.-260A=	ENSP00000501646.1:n.-260A=
ENST00000675194.1:n.69A=
ENST00000675298.1:c.-357A=	ENSP00000501839.1:n.-357A=
ENST00000675530.1:c.-353A=	ENSP00000501972.1:n.-353A=
ENST00000675817.1:c.-357A=	ENSP00000502422.1:n.-357A=
ENST00000675872.1:n.40A=
ENST00000675959.1:n.41A=
ENST00000676369.1:c.-425A=	ENSP00000502005.1:n.-425A=
ENST00000676426.1:c.-357A=	ENSP00000502359.1:n.-357A=
ENST00000444836.5:c.-212A=	ENSP00000416338.1:n.-212A=
NM_001127660.1:c.-212A=	NP_001121132.1:n.-212A=
NM_014874.3:c.-357A= , LRG_255t1:c.-357A=	NP_055689.1:n.-357A=
XM_005263543.2:c.-425A=	XP_005263600.1:n.-425A=
XM_005263548.2:c.-421A=	XP_005263605.1:n.-421A=
XM_005263543.3:c.-425A=	XP_005263600.1:n.-425A=
XM_005263548.3:c.-421A=	XP_005263605.1:n.-421A=