Canonical Allele Identifier: CA1153915795
Gene: MFN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11998782T= , CM000663.2:g.11998782T= GRCh38
NC_000001.10:g.12058839T= , CM000663.1:g.12058839T= GRCh37
NC_000001.9:g.11981426T= NCBI36
NG_007945.1:g.23602T= , LRG_255:g.23602T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235329.10:c.612T= MANE Select ENSP00000235329.5:p.Asp204=
ENST00000674548.1:c.612T= ENSP00000502185.1:p.Asp204=
ENST00000674658.1:c.267T= ENSP00000502334.1:p.Asp89=
ENST00000674706.1:n.1051T=
ENST00000674817.1:c.612T= ENSP00000502151.1:p.Asp204=
ENST00000674910.1:c.612T= ENSP00000501716.1:p.Asp204=
ENST00000675053.1:c.612T= ENSP00000501646.1:p.Asp204=
ENST00000675113.1:c.612T= ENSP00000502623.1:p.Asp204=
ENST00000675194.1:n.1037T=
ENST00000675231.1:c.612T= ENSP00000502404.1:p.Asp204=
ENST00000675298.1:c.612T= ENSP00000501839.1:p.Asp204=
ENST00000675374.1:n.302T=
ENST00000675483.1:n.740T=
ENST00000675512.1:c.*614T= ENSP00000502630.1:n.*614T=
ENST00000675528.1:n.103T=
ENST00000675817.1:c.612T= ENSP00000502422.1:p.Asp204=
ENST00000675872.1:n.863T=
ENST00000675919.1:c.612T= ENSP00000501776.1:p.Asp204=
ENST00000675959.1:n.1009T=
ENST00000675987.1:c.612T= ENSP00000502145.1:p.Asp204=
ENST00000676293.1:c.612T= ENSP00000502362.1:p.Asp204=
ENST00000676426.1:c.599+1361T= ENSP00000502359.1:n.599+1361T=
ENST00000235329.9:c.612T= ENSP00000235329.5:p.Asp204=
ENST00000444836.5:c.612T= ENSP00000416338.1:p.Asp204=
NM_001127660.1:c.612T= NP_001121132.1:p.Asp204=
NM_014874.3:c.612T= , LRG_255t1:c.612T= NP_055689.1:p.Asp204=
XM_005263543.2:c.612T= XP_005263600.1:p.Asp204=
XM_005263545.2:c.612T= XP_005263602.1:p.Asp204=
XM_005263547.2:c.612T= XP_005263604.1:p.Asp204=
XM_005263548.2:c.612T= XP_005263605.1:p.Asp204=
XM_005263543.3:c.612T= XP_005263600.1:p.Asp204=
XM_005263545.3:c.612T= XP_005263602.1:p.Asp204=
XM_005263547.3:c.612T= XP_005263604.1:p.Asp204=
XM_005263548.3:c.612T= XP_005263605.1:p.Asp204=
XM_024451299.1:c.612T= XP_024307067.1:p.Asp204=
NM_014874.4:c.612T= MANE Select NP_055689.1:p.Asp204=
NM_001127660.2:c.612T= NP_001121132.1:p.Asp204=