Canonical Allele Identifier: CA1153928243

Gene: MFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12007177_12007178delinsTG , CM000663.2:g.12007177_12007178delinsTG	GRCh38
NC_000001.10:g.12067234_12067235delinsTG , CM000663.1:g.12067234_12067235delinsTG	GRCh37
NC_000001.9:g.11989821_11989822delinsTG	NCBI36
NG_007945.1:g.31997_31998delinsTG , LRG_255:g.31997_31998delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.1997_1998delinsTG MANE Select	ENSP00000235329.5:p.Val666=
ENST00000674548.1:c.1997_1998delinsTG	ENSP00000502185.1:p.Val666=
ENST00000674658.1:c.1652_1653delinsTG	ENSP00000502334.1:p.Val551=
ENST00000674817.1:c.1997_1998delinsTG	ENSP00000502151.1:p.Val666=
ENST00000674910.1:c.1997_1998delinsTG	ENSP00000501716.1:p.Val666=
ENST00000675053.1:c.1997_1998delinsTG	ENSP00000501646.1:p.Val666=
ENST00000675113.1:c.1997_1998delinsTG	ENSP00000502623.1:p.Val666=
ENST00000675231.1:c.1997_1998delinsTG	ENSP00000502404.1:p.Val666=
ENST00000675298.1:c.1997_1998delinsTG	ENSP00000501839.1:p.Val666=
ENST00000675404.1:n.2232_2233delinsTG
ENST00000675483.1:n.2125_2126delinsTG
ENST00000675512.1:c.*1999_*2000delinsTG	ENSP00000502630.1:n.*1999_*2000delinsTG
ENST00000675528.1:n.1488_1489delinsTG
ENST00000675817.1:c.2129_2130delinsTG	ENSP00000502422.1:p.Val710=
ENST00000675872.1:n.2357_2358delinsTG
ENST00000675919.1:c.1997_1998delinsTG	ENSP00000501776.1:p.Val666=
ENST00000675959.1:n.2503_2504delinsTG
ENST00000675987.1:c.1997_1998delinsTG	ENSP00000502145.1:p.Val666=
ENST00000676293.1:c.1997_1998delinsTG	ENSP00000502362.1:p.Val666=
ENST00000676295.1:n.410_411delinsTG
ENST00000676426.1:c.*997_*998delinsTG	ENSP00000502359.1:n.*997_*998delinsTG
ENST00000235329.9:c.1997_1998delinsTG	ENSP00000235329.5:p.Val666=
ENST00000444836.5:c.1997_1998delinsTG	ENSP00000416338.1:p.Val666=
NM_001127660.1:c.1997_1998delinsTG	NP_001121132.1:p.Val666=
NM_014874.3:c.1997_1998delinsTG , LRG_255t1:c.1997_1998delinsTG	NP_055689.1:p.Val666=
XM_005263543.2:c.1997_1998delinsTG	XP_005263600.1:p.Val666=
XM_005263545.2:c.1997_1998delinsTG	XP_005263602.1:p.Val666=
XM_005263547.2:c.1997_1998delinsTG	XP_005263604.1:p.Val666=
XM_005263548.2:c.1997_1998delinsTG	XP_005263605.1:p.Val666=
XM_005263543.3:c.1997_1998delinsTG	XP_005263600.1:p.Val666=
XM_005263545.3:c.1997_1998delinsTG	XP_005263602.1:p.Val666=
XM_005263547.3:c.1997_1998delinsTG	XP_005263604.1:p.Val666=
XM_005263548.3:c.1997_1998delinsTG	XP_005263605.1:p.Val666=
XM_024451299.1:c.1997_1998delinsTG	XP_024307067.1:p.Val666=
NM_014874.4:c.1997_1998delinsTG MANE Select	NP_055689.1:p.Val666=
NM_001127660.2:c.1997_1998delinsTG	NP_001121132.1:p.Val666=