Canonical Allele Identifier: CA2643320909

Gene: MFN2

Linked Data

• gnomAD v4: 1-11980279-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980279G>T , CM000663.2:g.11980279G>T	GRCh38
NC_000001.10:g.12040336G>T , CM000663.1:g.12040336G>T	GRCh37
NC_000001.9:g.11962923G>T	NCBI36
NG_007945.1:g.5099G>T , LRG_255:g.5099G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-419G>T	ENSP00000412023.1:n.-419G>T
ENST00000674548.1:c.-300G>T	ENSP00000502185.1:n.-300G>T
ENST00000674658.1:c.-453G>T	ENSP00000502334.1:n.-453G>T
ENST00000674706.1:n.21G>T
ENST00000674817.1:c.-210G>T	ENSP00000502151.1:n.-210G>T
ENST00000675053.1:c.-258G>T	ENSP00000501646.1:n.-258G>T
ENST00000675194.1:n.71G>T
ENST00000675298.1:c.-355G>T	ENSP00000501839.1:n.-355G>T
ENST00000675530.1:c.-351G>T	ENSP00000501972.1:n.-351G>T
ENST00000675817.1:c.-355G>T	ENSP00000502422.1:n.-355G>T
ENST00000675872.1:n.42G>T
ENST00000675959.1:n.43G>T
ENST00000676369.1:c.-423G>T	ENSP00000502005.1:n.-423G>T
ENST00000676426.1:c.-355G>T	ENSP00000502359.1:n.-355G>T
ENST00000444836.5:c.-210G>T	ENSP00000416338.1:n.-210G>T
NM_001127660.1:c.-210G>T	NP_001121132.1:n.-210G>T
NM_014874.3:c.-355G>T , LRG_255t1:c.-355G>T	NP_055689.1:n.-355G>T
XM_005263543.2:c.-423G>T	XP_005263600.1:n.-423G>T
XM_005263548.2:c.-419G>T	XP_005263605.1:n.-419G>T
XM_005263543.3:c.-423G>T	XP_005263600.1:n.-423G>T
XM_005263548.3:c.-419G>T	XP_005263605.1:n.-419G>T