Canonical Allele Identifier: CA1153916296

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11998978_11998979delinsCT , CM000663.2:g.11998978_11998979delinsCT	GRCh38
NC_000001.10:g.12059035_12059036delinsCT , CM000663.1:g.12059035_12059036delinsCT	GRCh37
NC_000001.9:g.11981622_11981623delinsCT	NCBI36
NG_007945.1:g.23798_23799delinsCT , LRG_255:g.23798_23799delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000235329.10:c.709-10_709-9delinsCT MANE Select	ENSP00000235329.5:n.709-10_709-9delinsCT
ENST00000674548.1:c.709-10_709-9delinsCT	ENSP00000502185.1:n.709-10_709-9delinsCT
ENST00000674658.1:c.364-10_364-9delinsCT	ENSP00000502334.1:n.364-10_364-9delinsCT
ENST00000674706.1:n.1148-10_1148-9delinsCT
ENST00000674817.1:c.709-10_709-9delinsCT	ENSP00000502151.1:n.709-10_709-9delinsCT
ENST00000674910.1:c.709-10_709-9delinsCT	ENSP00000501716.1:n.709-10_709-9delinsCT
ENST00000675053.1:c.709-10_709-9delinsCT	ENSP00000501646.1:n.709-10_709-9delinsCT
ENST00000675113.1:c.709-10_709-9delinsCT	ENSP00000502623.1:n.709-10_709-9delinsCT
ENST00000675194.1:n.1134-10_1134-9delinsCT
ENST00000675231.1:c.709-10_709-9delinsCT	ENSP00000502404.1:n.709-10_709-9delinsCT
ENST00000675298.1:c.709-10_709-9delinsCT	ENSP00000501839.1:n.709-10_709-9delinsCT
ENST00000675374.1:n.498_499delinsCT
ENST00000675483.1:n.837-10_837-9delinsCT
ENST00000675512.1:c.*711-10_*711-9delinsCT	ENSP00000502630.1:n.*711-10_*711-9delinsC...
ENST00000675528.1:n.200-10_200-9delinsCT
ENST00000675817.1:c.709-10_709-9delinsCT	ENSP00000502422.1:n.709-10_709-9delinsCT
ENST00000675872.1:n.1059_1060delinsCT
ENST00000675919.1:c.709-10_709-9delinsCT	ENSP00000501776.1:n.709-10_709-9delinsCT
ENST00000675959.1:n.1205_1206delinsCT
ENST00000675987.1:c.709-10_709-9delinsCT	ENSP00000502145.1:n.709-10_709-9delinsCT
ENST00000676293.1:c.709-10_709-9delinsCT	ENSP00000502362.1:n.709-10_709-9delinsCT
ENST00000676426.1:c.599+1557_599+1558delinsCT	ENSP00000502359.1:n.599+1557_599+1558deli...
ENST00000235329.9:c.709-10_709-9delinsCT	ENSP00000235329.5:n.709-10_709-9delinsCT
ENST00000444836.5:c.709-10_709-9delinsCT	ENSP00000416338.1:n.709-10_709-9delinsCT
NM_001127660.1:c.709-10_709-9delinsCT	NP_001121132.1:n.709-10_709-9delinsCT
NM_014874.3:c.709-10_709-9delinsCT , LRG_255t1:c.709-10_709-9delinsCT	NP_055689.1:n.709-10_709-9delinsCT
XM_005263543.2:c.709-10_709-9delinsCT	XP_005263600.1:n.709-10_709-9delinsCT
XM_005263545.2:c.709-10_709-9delinsCT	XP_005263602.1:n.709-10_709-9delinsCT
XM_005263547.2:c.709-10_709-9delinsCT	XP_005263604.1:n.709-10_709-9delinsCT
XM_005263548.2:c.709-10_709-9delinsCT	XP_005263605.1:n.709-10_709-9delinsCT
XM_005263543.3:c.709-10_709-9delinsCT	XP_005263600.1:n.709-10_709-9delinsCT
XM_005263545.3:c.709-10_709-9delinsCT	XP_005263602.1:n.709-10_709-9delinsCT
XM_005263547.3:c.709-10_709-9delinsCT	XP_005263604.1:n.709-10_709-9delinsCT
XM_005263548.3:c.709-10_709-9delinsCT	XP_005263605.1:n.709-10_709-9delinsCT
XM_024451299.1:c.709-10_709-9delinsCT	XP_024307067.1:n.709-10_709-9delinsCT
NM_014874.4:c.709-10_709-9delinsCT MANE Select	NP_055689.1:n.709-10_709-9delinsCT
NM_001127660.2:c.709-10_709-9delinsCT	NP_001121132.1:n.709-10_709-9delinsCT