Canonical Allele Identifier: CA1153896931

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980392C= , CM000663.2:g.11980392C=	GRCh38
NC_000001.10:g.12040449C= , CM000663.1:g.12040449C=	GRCh37
NC_000001.9:g.11963036C=	NCBI36
NG_007945.1:g.5212C= , LRG_255:g.5212C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-306C=	ENSP00000412023.1:n.-306C=
ENST00000674548.1:c.-187C=	ENSP00000502185.1:n.-187C=
ENST00000674658.1:c.-340C=	ENSP00000502334.1:n.-340C=
ENST00000674706.1:n.134C=
ENST00000674817.1:c.-97C=	ENSP00000502151.1:n.-97C=
ENST00000674910.1:c.-219C=	ENSP00000501716.1:n.-219C=
ENST00000675053.1:c.-145C=	ENSP00000501646.1:n.-145C=
ENST00000675194.1:n.184C=
ENST00000675231.1:c.-470C=	ENSP00000502404.1:n.-470C=
ENST00000675298.1:c.-242C=	ENSP00000501839.1:n.-242C=
ENST00000675530.1:c.-238C=	ENSP00000501972.1:n.-238C=
ENST00000675817.1:c.-242C=	ENSP00000502422.1:n.-242C=
ENST00000675872.1:n.155C=
ENST00000675959.1:n.156C=
ENST00000676369.1:c.-310C=	ENSP00000502005.1:n.-310C=
ENST00000676426.1:c.-242C=	ENSP00000502359.1:n.-242C=
ENST00000235329.9:c.-242C=	ENSP00000235329.5:n.-242C=
ENST00000444836.5:c.-97C=	ENSP00000416338.1:n.-97C=
ENST00000484391.5:n.23C=
ENST00000490079.5:n.94C=
NM_001127660.1:c.-97C=	NP_001121132.1:n.-97C=
NM_014874.3:c.-242C= , LRG_255t1:c.-242C=	NP_055689.1:n.-242C=
XM_005263543.2:c.-310C=	XP_005263600.1:n.-310C=
XM_005263545.2:c.-238C=	XP_005263602.1:n.-238C=
XM_005263548.2:c.-306C=	XP_005263605.1:n.-306C=
XM_005263543.3:c.-310C=	XP_005263600.1:n.-310C=
XM_005263545.3:c.-238C=	XP_005263602.1:n.-238C=
XM_005263548.3:c.-306C=	XP_005263605.1:n.-306C=
XM_024451299.1:c.-470C=	XP_024307067.1:n.-470C=