Canonical Allele Identifier: CA2643320955

Gene: MFN2

Linked Data

• gnomAD v4: 1-11980321-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980321G>A , CM000663.2:g.11980321G>A	GRCh38
NC_000001.10:g.12040378G>A , CM000663.1:g.12040378G>A	GRCh37
NC_000001.9:g.11962965G>A	NCBI36
NG_007945.1:g.5141G>A , LRG_255:g.5141G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-377G>A	ENSP00000412023.1:n.-377G>A
ENST00000674548.1:c.-258G>A	ENSP00000502185.1:n.-258G>A
ENST00000674658.1:c.-411G>A	ENSP00000502334.1:n.-411G>A
ENST00000674706.1:n.63G>A
ENST00000674817.1:c.-168G>A	ENSP00000502151.1:n.-168G>A
ENST00000674910.1:c.-290G>A	ENSP00000501716.1:n.-290G>A
ENST00000675053.1:c.-216G>A	ENSP00000501646.1:n.-216G>A
ENST00000675194.1:n.113G>A
ENST00000675231.1:c.-541G>A	ENSP00000502404.1:n.-541G>A
ENST00000675298.1:c.-313G>A	ENSP00000501839.1:n.-313G>A
ENST00000675530.1:c.-309G>A	ENSP00000501972.1:n.-309G>A
ENST00000675817.1:c.-313G>A	ENSP00000502422.1:n.-313G>A
ENST00000675872.1:n.84G>A
ENST00000675959.1:n.85G>A
ENST00000676369.1:c.-381G>A	ENSP00000502005.1:n.-381G>A
ENST00000676426.1:c.-313G>A	ENSP00000502359.1:n.-313G>A
ENST00000235329.9:c.-313G>A	ENSP00000235329.5:n.-313G>A
ENST00000444836.5:c.-168G>A	ENSP00000416338.1:n.-168G>A
ENST00000490079.5:n.23G>A
NM_001127660.1:c.-168G>A	NP_001121132.1:n.-168G>A
NM_014874.3:c.-313G>A , LRG_255t1:c.-313G>A	NP_055689.1:n.-313G>A
XM_005263543.2:c.-381G>A	XP_005263600.1:n.-381G>A
XM_005263545.2:c.-309G>A	XP_005263602.1:n.-309G>A
XM_005263548.2:c.-377G>A	XP_005263605.1:n.-377G>A
XM_005263543.3:c.-381G>A	XP_005263600.1:n.-381G>A
XM_005263545.3:c.-309G>A	XP_005263602.1:n.-309G>A
XM_005263548.3:c.-377G>A	XP_005263605.1:n.-377G>A
XM_024451299.1:c.-541G>A	XP_024307067.1:n.-541G>A