Canonical Allele Identifier: CA2742488500

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12002272_12002273insA , CM000663.2:g.12002272_12002273insA	GRCh38
NC_000001.10:g.12062329_12062330insA , CM000663.1:g.12062329_12062330insA	GRCh37
NC_000001.9:g.11984916_11984917insA	NCBI36
NG_007945.1:g.27092_27093insA , LRG_255:g.27092_27093insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.1160+169_1160+170insA MANE Select	ENSP00000235329.5:n.1160+169_1160+170insA
ENST00000674548.1:c.1160+169_1160+170insA	ENSP00000502185.1:n.1160+169_1160+170insA
ENST00000674658.1:c.815+169_815+170insA	ENSP00000502334.1:n.815+169_815+170insA
ENST00000674817.1:c.1160+169_1160+170insA	ENSP00000502151.1:n.1160+169_1160+170insA
ENST00000674910.1:c.1160+169_1160+170insA	ENSP00000501716.1:n.1160+169_1160+170insA
ENST00000675053.1:c.1160+169_1160+170insA	ENSP00000501646.1:n.1160+169_1160+170insA
ENST00000675113.1:c.1160+169_1160+170insA	ENSP00000502623.1:n.1160+169_1160+170insA
ENST00000675194.1:n.1754_1755insA
ENST00000675231.1:c.1160+169_1160+170insA	ENSP00000502404.1:n.1160+169_1160+170insA
ENST00000675298.1:c.1160+169_1160+170insA	ENSP00000501839.1:n.1160+169_1160+170insA
ENST00000675404.1:n.1395+169_1395+170insA
ENST00000675483.1:n.1288+169_1288+170insA
ENST00000675512.1:c.*1162+169_*1162+170insA	ENSP00000502630.1:n.*1162+169_*1162+170insA
ENST00000675528.1:n.651+169_651+170insA
ENST00000675817.1:c.1160+169_1160+170insA	ENSP00000502422.1:n.1160+169_1160+170insA
ENST00000675872.1:n.1520+169_1520+170insA
ENST00000675919.1:c.1160+169_1160+170insA	ENSP00000501776.1:n.1160+169_1160+170insA
ENST00000675959.1:n.1666+169_1666+170insA
ENST00000675987.1:c.1160+169_1160+170insA	ENSP00000502145.1:n.1160+169_1160+170insA
ENST00000676293.1:c.1160+169_1160+170insA	ENSP00000502362.1:n.1160+169_1160+170insA
ENST00000676426.1:c.*160+169_*160+170insA	ENSP00000502359.1:n.*160+169_*160+170insA
ENST00000235329.9:c.1160+169_1160+170insA	ENSP00000235329.5:n.1160+169_1160+170insA
ENST00000444836.5:c.1160+169_1160+170insA	ENSP00000416338.1:n.1160+169_1160+170insA
NM_001127660.1:c.1160+169_1160+170insA	NP_001121132.1:n.1160+169_1160+170insA
NM_014874.3:c.1160+169_1160+170insA , LRG_255t1:c.1160+169_1160+170insA	NP_055689.1:n.1160+169_1160+170insA
XM_005263543.2:c.1160+169_1160+170insA	XP_005263600.1:n.1160+169_1160+170insA
XM_005263545.2:c.1160+169_1160+170insA	XP_005263602.1:n.1160+169_1160+170insA
XM_005263547.2:c.1160+169_1160+170insA	XP_005263604.1:n.1160+169_1160+170insA
XM_005263548.2:c.1160+169_1160+170insA	XP_005263605.1:n.1160+169_1160+170insA
XM_005263543.3:c.1160+169_1160+170insA	XP_005263600.1:n.1160+169_1160+170insA
XM_005263545.3:c.1160+169_1160+170insA	XP_005263602.1:n.1160+169_1160+170insA
XM_005263547.3:c.1160+169_1160+170insA	XP_005263604.1:n.1160+169_1160+170insA
XM_005263548.3:c.1160+169_1160+170insA	XP_005263605.1:n.1160+169_1160+170insA
XM_024451299.1:c.1160+169_1160+170insA	XP_024307067.1:n.1160+169_1160+170insA
NM_014874.4:c.1160+169_1160+170insA MANE Select	NP_055689.1:n.1160+169_1160+170insA
NM_001127660.2:c.1160+169_1160+170insA	NP_001121132.1:n.1160+169_1160+170insA