Canonical Allele Identifier: CA886272246

Gene: MFN2

Linked Data

• dbSNP Id: rs1281893384
• gnomAD v3: 1-11992146-CAAGG-C
• gnomAD v4: 1-11992146-CAAGG-C
• MyVariant Identifiers: chr1:g.12052204_12052207del (hg19) ; chr1:g.11992147_11992150del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11992151_11992154del , CM000663.2:g.11992151_11992154del	GRCh38
NC_000001.10:g.12052208_12052211del , CM000663.1:g.12052208_12052211del	GRCh37
NC_000001.9:g.11974795_11974798del	NCBI36
NG_007945.1:g.16971_16974del , LRG_255:g.16971_16974del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.176-404_176-401del MANE Select	ENSP00000235329.5:n.176-404_176-401del
ENST00000412236.2:c.176-404_176-401del	ENSP00000412023.1:n.176-404_176-401del
ENST00000674548.1:c.176-404_176-401del	ENSP00000502185.1:n.176-404_176-401del
ENST00000674658.1:c.-34-4005_-34-4002del	ENSP00000502334.1:n.-34-4005_-34-4002del
ENST00000674706.1:n.615-404_615-401del
ENST00000674817.1:c.176-404_176-401del	ENSP00000502151.1:n.176-404_176-401del
ENST00000674910.1:c.176-404_176-401del	ENSP00000501716.1:n.176-404_176-401del
ENST00000675053.1:c.176-404_176-401del	ENSP00000501646.1:n.176-404_176-401del
ENST00000675113.1:c.176-404_176-401del	ENSP00000502623.1:n.176-404_176-401del
ENST00000675194.1:n.601-404_601-401del
ENST00000675231.1:c.176-404_176-401del	ENSP00000502404.1:n.176-404_176-401del
ENST00000675298.1:c.176-404_176-401del	ENSP00000501839.1:n.176-404_176-401del
ENST00000675512.1:c.176-128_176-125del	ENSP00000502630.1:n.176-128_176-125del
ENST00000675530.1:c.176-404_176-401del	ENSP00000501972.1:n.176-404_176-401del
ENST00000675781.1:c.176-404_176-401del	ENSP00000501947.1:n.176-404_176-401del
ENST00000675817.1:c.176-404_176-401del	ENSP00000502422.1:n.176-404_176-401del
ENST00000675872.1:n.427-404_427-401del
ENST00000675919.1:c.176-404_176-401del	ENSP00000501776.1:n.176-404_176-401del
ENST00000675959.1:n.573-404_573-401del
ENST00000675987.1:c.176-404_176-401del	ENSP00000502145.1:n.176-404_176-401del
ENST00000676293.1:c.176-404_176-401del	ENSP00000502362.1:n.176-404_176-401del
ENST00000676369.1:c.176-404_176-401del	ENSP00000502005.1:n.176-404_176-401del
ENST00000676426.1:c.176-404_176-401del	ENSP00000502359.1:n.176-404_176-401del
ENST00000235329.9:c.176-404_176-401del	ENSP00000235329.5:n.176-404_176-401del
ENST00000412236.1:c.176-404_176-401del	ENSP00000412023.1:n.176-404_176-401del
ENST00000444836.5:c.176-404_176-401del	ENSP00000416338.1:n.176-404_176-401del
ENST00000497302.1:n.375-128_375-125del
NM_001127660.1:c.176-404_176-401del	NP_001121132.1:n.176-404_176-401del
NM_014874.3:c.176-404_176-401del , LRG_255t1:c.176-404_176-401del	NP_055689.1:n.176-404_176-401del
XM_005263543.2:c.176-404_176-401del	XP_005263600.1:n.176-404_176-401del
XM_005263545.2:c.176-404_176-401del	XP_005263602.1:n.176-404_176-401del
XM_005263547.2:c.176-404_176-401del	XP_005263604.1:n.176-404_176-401del
XM_005263548.2:c.176-404_176-401del	XP_005263605.1:n.176-404_176-401del
XM_005263543.3:c.176-404_176-401del	XP_005263600.1:n.176-404_176-401del
XM_005263545.3:c.176-404_176-401del	XP_005263602.1:n.176-404_176-401del
XM_005263547.3:c.176-404_176-401del	XP_005263604.1:n.176-404_176-401del
XM_005263548.3:c.176-404_176-401del	XP_005263605.1:n.176-404_176-401del
XM_024451299.1:c.176-404_176-401del	XP_024307067.1:n.176-404_176-401del
NM_014874.4:c.176-404_176-401del MANE Select	NP_055689.1:n.176-404_176-401del
NM_001127660.2:c.176-404_176-401del	NP_001121132.1:n.176-404_176-401del