Canonical Allele Identifier: CA1153919883

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12001677_12001685delinsTGCTCTTTA , CM000663.2:g.12001677_12001685delinsTGCTCTTTA	GRCh38
NC_000001.10:g.12061734_12061742delinsTGCTCTTTA , CM000663.1:g.12061734_12061742delinsTGCTCTTTA	GRCh37
NC_000001.9:g.11984321_11984329delinsTGCTCTTTA	NCBI36
NG_007945.1:g.26497_26505delinsTGCTCTTTA , LRG_255:g.26497_26505delinsTGCTCTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.971-92_971-84delinsTGCTCTTTA MANE Select	ENSP00000235329.5:n.971-92_971-84delinsTGCTCTTTA
ENST00000674548.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000502185.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000674658.1:c.626-92_626-84delinsTGCTCTTTA	ENSP00000502334.1:n.626-92_626-84delinsTGCTCTTTA
ENST00000674817.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000502151.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000674910.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000501716.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000675053.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000501646.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000675113.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000502623.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000675194.1:n.1396-92_1396-84delinsTGCTCTTTA
ENST00000675231.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000502404.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000675298.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000501839.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000675404.1:n.1206-92_1206-84delinsTGCTCTTTA
ENST00000675483.1:n.1099-92_1099-84delinsTGCTCTTTA
ENST00000675512.1:c.*973-92_*973-84delinsTGCTCTTTA	ENSP00000502630.1:n.*973-92_*973-84delinsTGCTCTTTA
ENST00000675528.1:n.462-92_462-84delinsTGCTCTTTA
ENST00000675817.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000502422.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000675872.1:n.1331-92_1331-84delinsTGCTCTTTA
ENST00000675919.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000501776.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000675959.1:n.1477-92_1477-84delinsTGCTCTTTA
ENST00000675987.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000502145.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000676293.1:c.971-92_971-84delinsTGCTCTTTA	ENSP00000502362.1:n.971-92_971-84delinsTGCTCTTTA
ENST00000676426.1:c.754-107_754-99delinsTGCTCTTTA	ENSP00000502359.1:n.754-107_754-99delinsTGCTCTTTA
ENST00000235329.9:c.971-92_971-84delinsTGCTCTTTA	ENSP00000235329.5:n.971-92_971-84delinsTGCTCTTTA
ENST00000444836.5:c.971-92_971-84delinsTGCTCTTTA	ENSP00000416338.1:n.971-92_971-84delinsTGCTCTTTA
NM_001127660.1:c.971-92_971-84delinsTGCTCTTTA	NP_001121132.1:n.971-92_971-84delinsTGCTCTTTA
NM_014874.3:c.971-92_971-84delinsTGCTCTTTA , LRG_255t1:c.971-92_971-84delinsTGCTCTTTA	NP_055689.1:n.971-92_971-84delinsTGCTCTTTA
XM_005263543.2:c.971-92_971-84delinsTGCTCTTTA	XP_005263600.1:n.971-92_971-84delinsTGCTCTTTA
XM_005263545.2:c.971-92_971-84delinsTGCTCTTTA	XP_005263602.1:n.971-92_971-84delinsTGCTCTTTA
XM_005263547.2:c.971-92_971-84delinsTGCTCTTTA	XP_005263604.1:n.971-92_971-84delinsTGCTCTTTA
XM_005263548.2:c.971-92_971-84delinsTGCTCTTTA	XP_005263605.1:n.971-92_971-84delinsTGCTCTTTA
XM_005263543.3:c.971-92_971-84delinsTGCTCTTTA	XP_005263600.1:n.971-92_971-84delinsTGCTCTTTA
XM_005263545.3:c.971-92_971-84delinsTGCTCTTTA	XP_005263602.1:n.971-92_971-84delinsTGCTCTTTA
XM_005263547.3:c.971-92_971-84delinsTGCTCTTTA	XP_005263604.1:n.971-92_971-84delinsTGCTCTTTA
XM_005263548.3:c.971-92_971-84delinsTGCTCTTTA	XP_005263605.1:n.971-92_971-84delinsTGCTCTTTA
XM_024451299.1:c.971-92_971-84delinsTGCTCTTTA	XP_024307067.1:n.971-92_971-84delinsTGCTCTTTA
NM_014874.4:c.971-92_971-84delinsTGCTCTTTA MANE Select	NP_055689.1:n.971-92_971-84delinsTGCTCTTTA
NM_001127660.2:c.971-92_971-84delinsTGCTCTTTA	NP_001121132.1:n.971-92_971-84delinsTGCTCTTTA