Canonical Allele Identifier: CA2742489474

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009841_12009842insAC , CM000663.2:g.12009841_12009842insAC	GRCh38
NC_000001.10:g.12069898_12069899insAC , CM000663.1:g.12069898_12069899insAC	GRCh37
NC_000001.9:g.11992485_11992486insAC	NCBI36
NG_007945.1:g.34661_34662insAC , LRG_255:g.34661_34662insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2204+115_2204+116insAC MANE Select	ENSP00000235329.5:n.2204+115_2204+116insAC
ENST00000674548.1:c.2204+115_2204+116insAC	ENSP00000502185.1:n.2204+115_2204+116insAC
ENST00000674658.1:c.1859+115_1859+116insAC	ENSP00000502334.1:n.1859+115_1859+116insAC
ENST00000674817.1:c.2204+115_2204+116insAC	ENSP00000502151.1:n.2204+115_2204+116insAC
ENST00000674910.1:c.2204+115_2204+116insAC	ENSP00000501716.1:n.2204+115_2204+116insAC
ENST00000675043.1:n.172+115_172+116insAC
ENST00000675053.1:c.2204+115_2204+116insAC	ENSP00000501646.1:n.2204+115_2204+116insAC
ENST00000675113.1:c.2204+115_2204+116insAC	ENSP00000502623.1:n.2204+115_2204+116insAC
ENST00000675231.1:c.2204+115_2204+116insAC	ENSP00000502404.1:n.2204+115_2204+116insAC
ENST00000675298.1:c.2204+115_2204+116insAC	ENSP00000501839.1:n.2204+115_2204+116insAC
ENST00000675404.1:n.2439+115_2439+116insAC
ENST00000675483.1:n.2332+115_2332+116insAC
ENST00000675512.1:c.*2206+115_*2206+116insAC	ENSP00000502630.1:n.*2206+115_*2206+116insAC
ENST00000675528.1:n.1695+115_1695+116insAC
ENST00000675817.1:c.2336+115_2336+116insAC	ENSP00000502422.1:n.2336+115_2336+116insAC
ENST00000675872.1:n.2564+115_2564+116insAC
ENST00000675919.1:c.2204+115_2204+116insAC	ENSP00000501776.1:n.2204+115_2204+116insAC
ENST00000675959.1:n.2710+115_2710+116insAC
ENST00000675987.1:c.*177+115_*177+116insAC	ENSP00000502145.1:n.*177+115_*177+116insAC
ENST00000676293.1:c.2204+115_2204+116insAC	ENSP00000502362.1:n.2204+115_2204+116insAC
ENST00000676295.1:n.617+115_617+116insAC
ENST00000676426.1:c.*1204+115_*1204+116insAC	ENSP00000502359.1:n.*1204+115_*1204+116insAC
ENST00000235329.9:c.2204+115_2204+116insAC	ENSP00000235329.5:n.2204+115_2204+116insAC
ENST00000444836.5:c.2204+115_2204+116insAC	ENSP00000416338.1:n.2204+115_2204+116insAC
NM_001127660.1:c.2204+115_2204+116insAC	NP_001121132.1:n.2204+115_2204+116insAC
NM_014874.3:c.2204+115_2204+116insAC , LRG_255t1:c.2204+115_2204+116insAC	NP_055689.1:n.2204+115_2204+116insAC
XM_005263543.2:c.2204+115_2204+116insAC	XP_005263600.1:n.2204+115_2204+116insAC
XM_005263545.2:c.2204+115_2204+116insAC	XP_005263602.1:n.2204+115_2204+116insAC
XM_005263547.2:c.2204+115_2204+116insAC	XP_005263604.1:n.2204+115_2204+116insAC
XM_005263548.2:c.2204+115_2204+116insAC	XP_005263605.1:n.2204+115_2204+116insAC
XM_005263543.3:c.2204+115_2204+116insAC	XP_005263600.1:n.2204+115_2204+116insAC
XM_005263545.3:c.2204+115_2204+116insAC	XP_005263602.1:n.2204+115_2204+116insAC
XM_005263547.3:c.2204+115_2204+116insAC	XP_005263604.1:n.2204+115_2204+116insAC
XM_005263548.3:c.2204+115_2204+116insAC	XP_005263605.1:n.2204+115_2204+116insAC
XM_024451299.1:c.2204+115_2204+116insAC	XP_024307067.1:n.2204+115_2204+116insAC
NM_014874.4:c.2204+115_2204+116insAC MANE Select	NP_055689.1:n.2204+115_2204+116insAC
NM_001127660.2:c.2204+115_2204+116insAC	NP_001121132.1:n.2204+115_2204+116insAC