Canonical Allele Identifier: CA1153919917

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12001708_12001716delinsATTTCATCG , CM000663.2:g.12001708_12001716delinsATTTCATCG	GRCh38
NC_000001.10:g.12061765_12061773delinsATTTCATCG , CM000663.1:g.12061765_12061773delinsATTTCATCG	GRCh37
NC_000001.9:g.11984352_11984360delinsATTTCATCG	NCBI36
NG_007945.1:g.26528_26536delinsATTTCATCG , LRG_255:g.26528_26536delinsATTTCATCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.971-61_971-53delinsATTTCATCG MANE Select	ENSP00000235329.5:n.971-61_971-53delinsATTTCATCG
ENST00000674548.1:c.971-61_971-53delinsATTTCATCG	ENSP00000502185.1:n.971-61_971-53delinsATTTCATCG
ENST00000674658.1:c.626-61_626-53delinsATTTCATCG	ENSP00000502334.1:n.626-61_626-53delinsATTTCATCG
ENST00000674817.1:c.971-61_971-53delinsATTTCATCG	ENSP00000502151.1:n.971-61_971-53delinsATTTCATCG
ENST00000674910.1:c.971-61_971-53delinsATTTCATCG	ENSP00000501716.1:n.971-61_971-53delinsATTTCATCG
ENST00000675053.1:c.971-61_971-53delinsATTTCATCG	ENSP00000501646.1:n.971-61_971-53delinsATTTCATCG
ENST00000675113.1:c.971-61_971-53delinsATTTCATCG	ENSP00000502623.1:n.971-61_971-53delinsATTTCATCG
ENST00000675194.1:n.1396-61_1396-53delinsATTTCATCG
ENST00000675231.1:c.971-61_971-53delinsATTTCATCG	ENSP00000502404.1:n.971-61_971-53delinsATTTCATCG
ENST00000675298.1:c.971-61_971-53delinsATTTCATCG	ENSP00000501839.1:n.971-61_971-53delinsATTTCATCG
ENST00000675404.1:n.1206-61_1206-53delinsATTTCATCG
ENST00000675483.1:n.1099-61_1099-53delinsATTTCATCG
ENST00000675512.1:c.*973-61_*973-53delinsATTTCATCG	ENSP00000502630.1:n.*973-61_*973-53delinsATTTCATCG
ENST00000675528.1:n.462-61_462-53delinsATTTCATCG
ENST00000675817.1:c.971-61_971-53delinsATTTCATCG	ENSP00000502422.1:n.971-61_971-53delinsATTTCATCG
ENST00000675872.1:n.1331-61_1331-53delinsATTTCATCG
ENST00000675919.1:c.971-61_971-53delinsATTTCATCG	ENSP00000501776.1:n.971-61_971-53delinsATTTCATCG
ENST00000675959.1:n.1477-61_1477-53delinsATTTCATCG
ENST00000675987.1:c.971-61_971-53delinsATTTCATCG	ENSP00000502145.1:n.971-61_971-53delinsATTTCATCG
ENST00000676293.1:c.971-61_971-53delinsATTTCATCG	ENSP00000502362.1:n.971-61_971-53delinsATTTCATCG
ENST00000676426.1:c.754-76_754-68delinsATTTCATCG	ENSP00000502359.1:n.754-76_754-68delinsATTTCATCG
ENST00000235329.9:c.971-61_971-53delinsATTTCATCG	ENSP00000235329.5:n.971-61_971-53delinsATTTCATCG
ENST00000444836.5:c.971-61_971-53delinsATTTCATCG	ENSP00000416338.1:n.971-61_971-53delinsATTTCATCG
NM_001127660.1:c.971-61_971-53delinsATTTCATCG	NP_001121132.1:n.971-61_971-53delinsATTTCATCG
NM_014874.3:c.971-61_971-53delinsATTTCATCG , LRG_255t1:c.971-61_971-53delinsATTTCATCG	NP_055689.1:n.971-61_971-53delinsATTTCATCG
XM_005263543.2:c.971-61_971-53delinsATTTCATCG	XP_005263600.1:n.971-61_971-53delinsATTTCATCG
XM_005263545.2:c.971-61_971-53delinsATTTCATCG	XP_005263602.1:n.971-61_971-53delinsATTTCATCG
XM_005263547.2:c.971-61_971-53delinsATTTCATCG	XP_005263604.1:n.971-61_971-53delinsATTTCATCG
XM_005263548.2:c.971-61_971-53delinsATTTCATCG	XP_005263605.1:n.971-61_971-53delinsATTTCATCG
XM_005263543.3:c.971-61_971-53delinsATTTCATCG	XP_005263600.1:n.971-61_971-53delinsATTTCATCG
XM_005263545.3:c.971-61_971-53delinsATTTCATCG	XP_005263602.1:n.971-61_971-53delinsATTTCATCG
XM_005263547.3:c.971-61_971-53delinsATTTCATCG	XP_005263604.1:n.971-61_971-53delinsATTTCATCG
XM_005263548.3:c.971-61_971-53delinsATTTCATCG	XP_005263605.1:n.971-61_971-53delinsATTTCATCG
XM_024451299.1:c.971-61_971-53delinsATTTCATCG	XP_024307067.1:n.971-61_971-53delinsATTTCATCG
NM_014874.4:c.971-61_971-53delinsATTTCATCG MANE Select	NP_055689.1:n.971-61_971-53delinsATTTCATCG
NM_001127660.2:c.971-61_971-53delinsATTTCATCG	NP_001121132.1:n.971-61_971-53delinsATTTCATCG