Canonical Allele Identifier: CA1153896903

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980355C= , CM000663.2:g.11980355C=	GRCh38
NC_000001.10:g.12040412C= , CM000663.1:g.12040412C=	GRCh37
NC_000001.9:g.11962999C=	NCBI36
NG_007945.1:g.5175C= , LRG_255:g.5175C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-343C=	ENSP00000412023.1:n.-343C=
ENST00000674548.1:c.-224C=	ENSP00000502185.1:n.-224C=
ENST00000674658.1:c.-377C=	ENSP00000502334.1:n.-377C=
ENST00000674706.1:n.97C=
ENST00000674817.1:c.-134C=	ENSP00000502151.1:n.-134C=
ENST00000674910.1:c.-256C=	ENSP00000501716.1:n.-256C=
ENST00000675053.1:c.-182C=	ENSP00000501646.1:n.-182C=
ENST00000675194.1:n.147C=
ENST00000675231.1:c.-507C=	ENSP00000502404.1:n.-507C=
ENST00000675298.1:c.-279C=	ENSP00000501839.1:n.-279C=
ENST00000675530.1:c.-275C=	ENSP00000501972.1:n.-275C=
ENST00000675817.1:c.-279C=	ENSP00000502422.1:n.-279C=
ENST00000675872.1:n.118C=
ENST00000675959.1:n.119C=
ENST00000676369.1:c.-347C=	ENSP00000502005.1:n.-347C=
ENST00000676426.1:c.-279C=	ENSP00000502359.1:n.-279C=
ENST00000235329.9:c.-279C=	ENSP00000235329.5:n.-279C=
ENST00000444836.5:c.-134C=	ENSP00000416338.1:n.-134C=
ENST00000490079.5:n.57C=
NM_001127660.1:c.-134C=	NP_001121132.1:n.-134C=
NM_014874.3:c.-279C= , LRG_255t1:c.-279C=	NP_055689.1:n.-279C=
XM_005263543.2:c.-347C=	XP_005263600.1:n.-347C=
XM_005263545.2:c.-275C=	XP_005263602.1:n.-275C=
XM_005263548.2:c.-343C=	XP_005263605.1:n.-343C=
XM_005263543.3:c.-347C=	XP_005263600.1:n.-347C=
XM_005263545.3:c.-275C=	XP_005263602.1:n.-275C=
XM_005263548.3:c.-343C=	XP_005263605.1:n.-343C=
XM_024451299.1:c.-507C=	XP_024307067.1:n.-507C=