Canonical Allele Identifier: CA15077980
Gene: MFN2 HGNC NCBI

Linked Data

dbSNP Id: rs4240897

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11982698G>A , CM000663.2:g.11982698G>A GRCh38
NC_000001.10:g.12042755G>A , CM000663.1:g.12042755G>A GRCh37
NC_000001.9:g.11965342G>A NCBI36
NG_007945.1:g.7518G>A , LRG_255:g.7518G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000235329.10:c.-5+584G>A MANE Select ENSP00000235329.5:p.=
ENST00000412236.2:c.-5+108G>A ENSP00000412023.1:p.=
ENST00000674548.1:c.-95+2214G>A ENSP00000502185.1:p.=
ENST00000674658.1:c.-35+108G>A ENSP00000502334.1:p.=
ENST00000674706.1:n.435+108G>A
ENST00000674817.1:c.-5+2214G>A ENSP00000502151.1:p.=
ENST00000674910.1:c.-127+2214G>A ENSP00000501716.1:p.=
ENST00000675053.1:c.-5+584G>A ENSP00000501646.1:p.=
ENST00000675113.1:c.-67+584G>A ENSP00000502623.1:p.=
ENST00000675194.1:n.421+584G>A
ENST00000675231.1:c.-5+108G>A ENSP00000502404.1:p.=
ENST00000675298.1:c.-5+584G>A ENSP00000501839.1:p.=
ENST00000675512.1:c.-5+584G>A ENSP00000502630.1:p.=
ENST00000675530.1:c.-5+584G>A ENSP00000501972.1:p.=
ENST00000675781.1:c.-5+584G>A ENSP00000501947.1:p.=
ENST00000675817.1:c.-5+584G>A ENSP00000502422.1:p.=
ENST00000675872.1:n.247+2214G>A
ENST00000675919.1:c.-95+584G>A ENSP00000501776.1:p.=
ENST00000675959.1:n.393+584G>A
ENST00000675987.1:c.-5+584G>A ENSP00000502145.1:p.=
ENST00000676293.1:c.-127+584G>A ENSP00000502362.1:p.=
ENST00000676369.1:c.-5+108G>A ENSP00000502005.1:p.=
ENST00000676426.1:c.-5+584G>A ENSP00000502359.1:p.=
ENST00000235329.9:c.-5+584G>A ENSP00000235329.5:p.=
ENST00000412236.1:c.-5+108G>A ENSP00000412023.1:p.=
ENST00000444836.5:c.-5+2214G>A ENSP00000416338.1:p.=
ENST00000484391.5:n.115+2214G>A
ENST00000490079.5:n.375+584G>A
ENST00000497302.1:n.195+584G>A
NM_001127660.1:c.-5+2214G>A NP_001121132.1:p.=
NM_014874.3:c.-5+584G>A , LRG_255t1:c.-5+584G>A NP_055689.1:p.=
XM_005263543.2:c.-5+108G>A XP_005263600.1:p.=
XM_005263545.2:c.-5+584G>A XP_005263602.1:p.=
XM_005263547.2:c.-5+584G>A XP_005263604.1:p.=
XM_005263548.2:c.-5+108G>A XP_005263605.1:p.=
XM_005263543.3:c.-5+108G>A XP_005263600.1:p.=
XM_005263545.3:c.-5+584G>A XP_005263602.1:p.=
XM_005263547.3:c.-5+584G>A XP_005263604.1:p.=
XM_005263548.3:c.-5+108G>A XP_005263605.1:p.=
XM_024451299.1:c.-5+108G>A XP_024307067.1:p.=
NM_014874.4:c.-5+584G>A MANE Select NP_055689.1:p.=
NM_001127660.2:c.-5+2214G>A NP_001121132.1:p.=