Canonical Allele Identifier: CA1153916262
Gene: MFN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11998957C= , CM000663.2:g.11998957C= GRCh38
NC_000001.10:g.12059014C= , CM000663.1:g.12059014C= GRCh37
NC_000001.9:g.11981601C= NCBI36
NG_007945.1:g.23777C= , LRG_255:g.23777C=

Transcript Alleles

HGVS Amino-acid change
ENST00000235329.10:c.709-31C= MANE Select ENSP00000235329.5:n.709-31C=
ENST00000674548.1:c.709-31C= ENSP00000502185.1:n.709-31C=
ENST00000674658.1:c.364-31C= ENSP00000502334.1:n.364-31C=
ENST00000674706.1:n.1148-31C=
ENST00000674817.1:c.709-31C= ENSP00000502151.1:n.709-31C=
ENST00000674910.1:c.709-31C= ENSP00000501716.1:n.709-31C=
ENST00000675053.1:c.709-31C= ENSP00000501646.1:n.709-31C=
ENST00000675113.1:c.709-31C= ENSP00000502623.1:n.709-31C=
ENST00000675194.1:n.1134-31C=
ENST00000675231.1:c.709-31C= ENSP00000502404.1:n.709-31C=
ENST00000675298.1:c.709-31C= ENSP00000501839.1:n.709-31C=
ENST00000675374.1:n.477C=
ENST00000675483.1:n.837-31C=
ENST00000675512.1:c.*711-31C= ENSP00000502630.1:n.*711-31C=
ENST00000675528.1:n.200-31C=
ENST00000675817.1:c.709-31C= ENSP00000502422.1:n.709-31C=
ENST00000675872.1:n.1038C=
ENST00000675919.1:c.709-31C= ENSP00000501776.1:n.709-31C=
ENST00000675959.1:n.1184C=
ENST00000675987.1:c.709-31C= ENSP00000502145.1:n.709-31C=
ENST00000676293.1:c.709-31C= ENSP00000502362.1:n.709-31C=
ENST00000676426.1:c.599+1536C= ENSP00000502359.1:n.599+1536C=
ENST00000235329.9:c.709-31C= ENSP00000235329.5:n.709-31C=
ENST00000444836.5:c.709-31C= ENSP00000416338.1:n.709-31C=
NM_001127660.1:c.709-31C= NP_001121132.1:n.709-31C=
NM_014874.3:c.709-31C= , LRG_255t1:c.709-31C= NP_055689.1:n.709-31C=
XM_005263543.2:c.709-31C= XP_005263600.1:n.709-31C=
XM_005263545.2:c.709-31C= XP_005263602.1:n.709-31C=
XM_005263547.2:c.709-31C= XP_005263604.1:n.709-31C=
XM_005263548.2:c.709-31C= XP_005263605.1:n.709-31C=
XM_005263543.3:c.709-31C= XP_005263600.1:n.709-31C=
XM_005263545.3:c.709-31C= XP_005263602.1:n.709-31C=
XM_005263547.3:c.709-31C= XP_005263604.1:n.709-31C=
XM_005263548.3:c.709-31C= XP_005263605.1:n.709-31C=
XM_024451299.1:c.709-31C= XP_024307067.1:n.709-31C=
NM_014874.4:c.709-31C= MANE Select NP_055689.1:n.709-31C=
NM_001127660.2:c.709-31C= NP_001121132.1:n.709-31C=