Canonical Allele Identifier: CA915941136

Gene: MFN2

Linked Data

• ClinVar Variation Id: 637310
• ClinVar RCV Id: RCV000789410

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12002100_12002101delinsCT , CM000663.2:g.12002100_12002101delinsCT	GRCh38
NC_000001.10:g.12062157_12062158delinsCT , CM000663.1:g.12062157_12062158delinsCT	GRCh37
NC_000001.9:g.11984744_11984745delinsCT	NCBI36
NG_007945.1:g.26920_26921delinsCT , LRG_255:g.26920_26921delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.1157_1158delinsCT MANE Select	ENSP00000235329.5:p.Gln386Pro
ENST00000674548.1:c.1157_1158delinsCT	ENSP00000502185.1:p.Gln386Pro
ENST00000674658.1:c.812_813delinsCT	ENSP00000502334.1:p.Gln271Pro
ENST00000674817.1:c.1157_1158delinsCT	ENSP00000502151.1:p.Gln386Pro
ENST00000674910.1:c.1157_1158delinsCT	ENSP00000501716.1:p.Gln386Pro
ENST00000675053.1:c.1157_1158delinsCT	ENSP00000501646.1:p.Gln386Pro
ENST00000675113.1:c.1157_1158delinsCT	ENSP00000502623.1:p.Gln386Pro
ENST00000675194.1:n.1582_1583delinsCT
ENST00000675231.1:c.1157_1158delinsCT	ENSP00000502404.1:p.Gln386Pro
ENST00000675298.1:c.1157_1158delinsCT	ENSP00000501839.1:p.Gln386Pro
ENST00000675404.1:n.1392_1393delinsCT
ENST00000675483.1:n.1285_1286delinsCT
ENST00000675512.1:c.*1159_*1160delinsCT	ENSP00000502630.1:n.*1159_*1160delinsCT
ENST00000675528.1:n.648_649delinsCT
ENST00000675817.1:c.1157_1158delinsCT	ENSP00000502422.1:p.Gln386Pro
ENST00000675872.1:n.1517_1518delinsCT
ENST00000675919.1:c.1157_1158delinsCT	ENSP00000501776.1:p.Gln386Pro
ENST00000675959.1:n.1663_1664delinsCT
ENST00000675987.1:c.1157_1158delinsCT	ENSP00000502145.1:p.Gln386Pro
ENST00000676293.1:c.1157_1158delinsCT	ENSP00000502362.1:p.Gln386Pro
ENST00000676426.1:c.*157_*158delinsCT	ENSP00000502359.1:n.*157_*158delinsCT
ENST00000235329.9:c.1157_1158delinsCT	ENSP00000235329.5:p.Gln386Pro
ENST00000444836.5:c.1157_1158delinsCT	ENSP00000416338.1:p.Gln386Pro
NM_001127660.1:c.1157_1158delinsCT	NP_001121132.1:p.Gln386Pro
NM_014874.3:c.1157_1158delinsCT , LRG_255t1:c.1157_1158delinsCT	NP_055689.1:p.Gln386Pro
XM_005263543.2:c.1157_1158delinsCT	XP_005263600.1:p.Gln386Pro
XM_005263545.2:c.1157_1158delinsCT	XP_005263602.1:p.Gln386Pro
XM_005263547.2:c.1157_1158delinsCT	XP_005263604.1:p.Gln386Pro
XM_005263548.2:c.1157_1158delinsCT	XP_005263605.1:p.Gln386Pro
XM_005263543.3:c.1157_1158delinsCT	XP_005263600.1:p.Gln386Pro
XM_005263545.3:c.1157_1158delinsCT	XP_005263602.1:p.Gln386Pro
XM_005263547.3:c.1157_1158delinsCT	XP_005263604.1:p.Gln386Pro
XM_005263548.3:c.1157_1158delinsCT	XP_005263605.1:p.Gln386Pro
XM_024451299.1:c.1157_1158delinsCT	XP_024307067.1:p.Gln386Pro
NM_014874.4:c.1157_1158delinsCT MANE Select	NP_055689.1:p.Gln386Pro
NM_001127660.2:c.1157_1158delinsCT	NP_001121132.1:p.Gln386Pro