Canonical Allele Identifier: CA2742488235
Gene: MFN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11999239_11999240insACA , CM000663.2:g.11999239_11999240insACA GRCh38
NC_000001.10:g.12059296_12059297insACA , CM000663.1:g.12059296_12059297insACA GRCh37
NC_000001.9:g.11981883_11981884insACA NCBI36
NG_007945.1:g.24059_24060insACA , LRG_255:g.24059_24060insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000235329.10:c.816+144_816+145insACA MANE Select ENSP00000235329.5:n.816+144_816+145insACA
ENST00000674548.1:c.816+144_816+145insACA ENSP00000502185.1:n.816+144_816+145insACA
ENST00000674658.1:c.471+144_471+145insACA ENSP00000502334.1:n.471+144_471+145insACA
ENST00000674706.1:n.1399_1400insACA
ENST00000674817.1:c.816+144_816+145insACA ENSP00000502151.1:n.816+144_816+145insACA
ENST00000674910.1:c.816+144_816+145insACA ENSP00000501716.1:n.816+144_816+145insACA
ENST00000675053.1:c.816+144_816+145insACA ENSP00000501646.1:n.816+144_816+145insACA
ENST00000675113.1:c.816+144_816+145insACA ENSP00000502623.1:n.816+144_816+145insACA
ENST00000675194.1:n.1241+144_1241+145insACA
ENST00000675231.1:c.816+144_816+145insACA ENSP00000502404.1:n.816+144_816+145insACA
ENST00000675298.1:c.816+144_816+145insACA ENSP00000501839.1:n.816+144_816+145insACA
ENST00000675483.1:n.944+144_944+145insACA
ENST00000675512.1:c.*818+144_*818+145insACA ENSP00000502630.1:n.*818+144_*818+145insACA
ENST00000675528.1:n.307+144_307+145insACA
ENST00000675817.1:c.816+144_816+145insACA ENSP00000502422.1:n.816+144_816+145insACA
ENST00000675872.1:n.1176+144_1176+145insACA
ENST00000675919.1:c.816+144_816+145insACA ENSP00000501776.1:n.816+144_816+145insACA
ENST00000675959.1:n.1322+144_1322+145insACA
ENST00000675987.1:c.816+144_816+145insACA ENSP00000502145.1:n.816+144_816+145insACA
ENST00000676293.1:c.816+144_816+145insACA ENSP00000502362.1:n.816+144_816+145insACA
ENST00000676426.1:c.599+1818_599+1819insACA ENSP00000502359.1:n.599+1818_599+1819insACA
ENST00000235329.9:c.816+144_816+145insACA ENSP00000235329.5:n.816+144_816+145insACA
ENST00000444836.5:c.816+144_816+145insACA ENSP00000416338.1:n.816+144_816+145insACA
NM_001127660.1:c.816+144_816+145insACA NP_001121132.1:n.816+144_816+145insACA
NM_014874.3:c.816+144_816+145insACA , LRG_255t1:c.816+144_816+145insACA NP_055689.1:n.816+144_816+145insACA
XM_005263543.2:c.816+144_816+145insACA XP_005263600.1:n.816+144_816+145insACA
XM_005263545.2:c.816+144_816+145insACA XP_005263602.1:n.816+144_816+145insACA
XM_005263547.2:c.816+144_816+145insACA XP_005263604.1:n.816+144_816+145insACA
XM_005263548.2:c.816+144_816+145insACA XP_005263605.1:n.816+144_816+145insACA
XM_005263543.3:c.816+144_816+145insACA XP_005263600.1:n.816+144_816+145insACA
XM_005263545.3:c.816+144_816+145insACA XP_005263602.1:n.816+144_816+145insACA
XM_005263547.3:c.816+144_816+145insACA XP_005263604.1:n.816+144_816+145insACA
XM_005263548.3:c.816+144_816+145insACA XP_005263605.1:n.816+144_816+145insACA
XM_024451299.1:c.816+144_816+145insACA XP_024307067.1:n.816+144_816+145insACA
NM_014874.4:c.816+144_816+145insACA MANE Select NP_055689.1:n.816+144_816+145insACA
NM_001127660.2:c.816+144_816+145insACA NP_001121132.1:n.816+144_816+145insACA