Canonical Allele Identifier: CA886277439

Gene: MFN2

Linked Data

• dbSNP Id: rs1490242463
• MyVariant Identifiers: chr1:g.12059364_12059366del (hg19) ; chr1:g.11999307_11999309del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11999308_11999310del , CM000663.2:g.11999308_11999310del	GRCh38
NC_000001.10:g.12059365_12059367del , CM000663.1:g.12059365_12059367del	GRCh37
NC_000001.9:g.11981952_11981954del	NCBI36
NG_007945.1:g.24128_24130del , LRG_255:g.24128_24130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.816+213_816+215del MANE Select	ENSP00000235329.5:n.816+213_816+215del
ENST00000674548.1:c.816+213_816+215del	ENSP00000502185.1:n.816+213_816+215del
ENST00000674658.1:c.471+213_471+215del	ENSP00000502334.1:n.471+213_471+215del
ENST00000674706.1:n.1468_1470del
ENST00000674817.1:c.816+213_816+215del	ENSP00000502151.1:n.816+213_816+215del
ENST00000674910.1:c.816+213_816+215del	ENSP00000501716.1:n.816+213_816+215del
ENST00000675053.1:c.816+213_816+215del	ENSP00000501646.1:n.816+213_816+215del
ENST00000675113.1:c.816+213_816+215del	ENSP00000502623.1:n.816+213_816+215del
ENST00000675194.1:n.1241+213_1241+215del
ENST00000675231.1:c.816+213_816+215del	ENSP00000502404.1:n.816+213_816+215del
ENST00000675298.1:c.816+213_816+215del	ENSP00000501839.1:n.816+213_816+215del
ENST00000675483.1:n.944+213_944+215del
ENST00000675512.1:c.*818+213_*818+215del	ENSP00000502630.1:n.*818+213_*818+215del
ENST00000675528.1:n.307+213_307+215del
ENST00000675817.1:c.816+213_816+215del	ENSP00000502422.1:n.816+213_816+215del
ENST00000675872.1:n.1176+213_1176+215del
ENST00000675919.1:c.816+213_816+215del	ENSP00000501776.1:n.816+213_816+215del
ENST00000675959.1:n.1322+213_1322+215del
ENST00000675987.1:c.816+213_816+215del	ENSP00000502145.1:n.816+213_816+215del
ENST00000676293.1:c.816+213_816+215del	ENSP00000502362.1:n.816+213_816+215del
ENST00000676426.1:c.599+1887_599+1889del	ENSP00000502359.1:n.599+1887_599+1889del
ENST00000235329.9:c.816+213_816+215del	ENSP00000235329.5:n.816+213_816+215del
ENST00000444836.5:c.816+213_816+215del	ENSP00000416338.1:n.816+213_816+215del
NM_001127660.1:c.816+213_816+215del	NP_001121132.1:n.816+213_816+215del
NM_014874.3:c.816+213_816+215del , LRG_255t1:c.816+213_816+215del	NP_055689.1:n.816+213_816+215del
XM_005263543.2:c.816+213_816+215del	XP_005263600.1:n.816+213_816+215del
XM_005263545.2:c.816+213_816+215del	XP_005263602.1:n.816+213_816+215del
XM_005263547.2:c.816+213_816+215del	XP_005263604.1:n.816+213_816+215del
XM_005263548.2:c.816+213_816+215del	XP_005263605.1:n.816+213_816+215del
XM_005263543.3:c.816+213_816+215del	XP_005263600.1:n.816+213_816+215del
XM_005263545.3:c.816+213_816+215del	XP_005263602.1:n.816+213_816+215del
XM_005263547.3:c.816+213_816+215del	XP_005263604.1:n.816+213_816+215del
XM_005263548.3:c.816+213_816+215del	XP_005263605.1:n.816+213_816+215del
XM_024451299.1:c.816+213_816+215del	XP_024307067.1:n.816+213_816+215del
NM_014874.4:c.816+213_816+215del MANE Select	NP_055689.1:n.816+213_816+215del
NM_001127660.2:c.816+213_816+215del	NP_001121132.1:n.816+213_816+215del