Canonical Allele Identifier: CA129420
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30736
dbSNP Id: rs387906990
gnomAD v2: 1-12058874-T-C
gnomAD v3: 1-11998817-T-C
gnomAD v4: 1-11998817-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11998817T>C , CM000663.2:g.11998817T>C GRCh38
NC_000001.10:g.12058874T>C , CM000663.1:g.12058874T>C GRCh37
NC_000001.9:g.11981461T>C NCBI36
NG_007945.1:g.23637T>C , LRG_255:g.23637T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235329.10:c.647T>C MANE Select ENSP00000235329.5:p.Phe216Ser
ENST00000674548.1:c.647T>C ENSP00000502185.1:p.Phe216Ser
ENST00000674658.1:c.302T>C ENSP00000502334.1:p.Phe101Ser
ENST00000674706.1:n.1086T>C
ENST00000674817.1:c.647T>C ENSP00000502151.1:p.Phe216Ser
ENST00000674910.1:c.647T>C ENSP00000501716.1:p.Phe216Ser
ENST00000675053.1:c.647T>C ENSP00000501646.1:p.Phe216Ser
ENST00000675113.1:c.647T>C ENSP00000502623.1:p.Phe216Ser
ENST00000675194.1:n.1072T>C
ENST00000675231.1:c.647T>C ENSP00000502404.1:p.Phe216Ser
ENST00000675298.1:c.647T>C ENSP00000501839.1:p.Phe216Ser
ENST00000675374.1:n.337T>C
ENST00000675483.1:n.775T>C
ENST00000675512.1:c.*649T>C ENSP00000502630.1:n.*649T>C
ENST00000675528.1:n.138T>C
ENST00000675817.1:c.647T>C ENSP00000502422.1:p.Phe216Ser
ENST00000675872.1:n.898T>C
ENST00000675919.1:c.647T>C ENSP00000501776.1:p.Phe216Ser
ENST00000675959.1:n.1044T>C
ENST00000675987.1:c.647T>C ENSP00000502145.1:p.Phe216Ser
ENST00000676293.1:c.647T>C ENSP00000502362.1:p.Phe216Ser
ENST00000676426.1:c.599+1396T>C ENSP00000502359.1:n.599+1396T>C
ENST00000235329.9:c.647T>C ENSP00000235329.5:p.Phe216Ser
ENST00000444836.5:c.647T>C ENSP00000416338.1:p.Phe216Ser
NM_001127660.1:c.647T>C NP_001121132.1:p.Phe216Ser
NM_014874.3:c.647T>C , LRG_255t1:c.647T>C NP_055689.1:p.Phe216Ser
XM_005263543.2:c.647T>C XP_005263600.1:p.Phe216Ser
XM_005263545.2:c.647T>C XP_005263602.1:p.Phe216Ser
XM_005263547.2:c.647T>C XP_005263604.1:p.Phe216Ser
XM_005263548.2:c.647T>C XP_005263605.1:p.Phe216Ser
XM_005263543.3:c.647T>C XP_005263600.1:p.Phe216Ser
XM_005263545.3:c.647T>C XP_005263602.1:p.Phe216Ser
XM_005263547.3:c.647T>C XP_005263604.1:p.Phe216Ser
XM_005263548.3:c.647T>C XP_005263605.1:p.Phe216Ser
XM_024451299.1:c.647T>C XP_024307067.1:p.Phe216Ser
NM_014874.4:c.647T>C MANE Select NP_055689.1:p.Phe216Ser
NM_001127660.2:c.647T>C NP_001121132.1:p.Phe216Ser