Canonical Allele Identifier: CA998640414
Gene: MFN2 HGNC NCBI

Linked Data

dbSNP Id: rs1645957536
gnomAD v3: 1-11980331-T-A
gnomAD v4: 1-11980331-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11980331T>A , CM000663.2:g.11980331T>A GRCh38
NC_000001.10:g.12040388T>A , CM000663.1:g.12040388T>A GRCh37
NC_000001.9:g.11962975T>A NCBI36
NG_007945.1:g.5151T>A , LRG_255:g.5151T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000412236.2:c.-367T>A ENSP00000412023.1:n.-367T>A
ENST00000674548.1:c.-248T>A ENSP00000502185.1:n.-248T>A
ENST00000674658.1:c.-401T>A ENSP00000502334.1:n.-401T>A
ENST00000674706.1:n.73T>A
ENST00000674817.1:c.-158T>A ENSP00000502151.1:n.-158T>A
ENST00000674910.1:c.-280T>A ENSP00000501716.1:n.-280T>A
ENST00000675053.1:c.-206T>A ENSP00000501646.1:n.-206T>A
ENST00000675194.1:n.123T>A
ENST00000675231.1:c.-531T>A ENSP00000502404.1:n.-531T>A
ENST00000675298.1:c.-303T>A ENSP00000501839.1:n.-303T>A
ENST00000675530.1:c.-299T>A ENSP00000501972.1:n.-299T>A
ENST00000675817.1:c.-303T>A ENSP00000502422.1:n.-303T>A
ENST00000675872.1:n.94T>A
ENST00000675959.1:n.95T>A
ENST00000676369.1:c.-371T>A ENSP00000502005.1:n.-371T>A
ENST00000676426.1:c.-303T>A ENSP00000502359.1:n.-303T>A
ENST00000235329.9:c.-303T>A ENSP00000235329.5:n.-303T>A
ENST00000444836.5:c.-158T>A ENSP00000416338.1:n.-158T>A
ENST00000490079.5:n.33T>A
NM_001127660.1:c.-158T>A NP_001121132.1:n.-158T>A
NM_014874.3:c.-303T>A , LRG_255t1:c.-303T>A NP_055689.1:n.-303T>A
XM_005263543.2:c.-371T>A XP_005263600.1:n.-371T>A
XM_005263545.2:c.-299T>A XP_005263602.1:n.-299T>A
XM_005263548.2:c.-367T>A XP_005263605.1:n.-367T>A
XM_005263543.3:c.-371T>A XP_005263600.1:n.-371T>A
XM_005263545.3:c.-299T>A XP_005263602.1:n.-299T>A
XM_005263548.3:c.-367T>A XP_005263605.1:n.-367T>A
XM_024451299.1:c.-531T>A XP_024307067.1:n.-531T>A