Canonical Allele Identifier: CA521184966

Gene: MFN2

Linked Data

• dbSNP Id: rs1199036756
• gnomAD v2: 1-12069232-CAGAGGGAGACCGTGGAAAGAGAGGG-C
• gnomAD v3: 1-12009175-CAGAGGGAGACCGTGGAAAGAGAGGG-C
• gnomAD v4: 1-12009175-CAGAGGGAGACCGTGGAAAGAGAGGG-C
• MyVariant Identifiers: chr1:g.12069233_12069257del (hg19) ; chr1:g.12009176_12009200del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009191_12009215del , CM000663.2:g.12009191_12009215del	GRCh38
NC_000001.10:g.12069248_12069272del , CM000663.1:g.12069248_12069272del	GRCh37
NC_000001.9:g.11991835_11991859del	NCBI36
NG_007945.1:g.34011_34035del , LRG_255:g.34011_34035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2070-401_2070-377del MANE Select	ENSP00000235329.5:n.2070-401_2070-377del
ENST00000674548.1:c.2070-401_2070-377del	ENSP00000502185.1:n.2070-401_2070-377del
ENST00000674658.1:c.1725-401_1725-377del	ENSP00000502334.1:n.1725-401_1725-377del
ENST00000674817.1:c.2070-401_2070-377del	ENSP00000502151.1:n.2070-401_2070-377del
ENST00000674910.1:c.2070-401_2070-377del	ENSP00000501716.1:n.2070-401_2070-377del
ENST00000675053.1:c.2070-401_2070-377del	ENSP00000501646.1:n.2070-401_2070-377del
ENST00000675113.1:c.2070-401_2070-377del	ENSP00000502623.1:n.2070-401_2070-377del
ENST00000675231.1:c.2070-401_2070-377del	ENSP00000502404.1:n.2070-401_2070-377del
ENST00000675298.1:c.2070-401_2070-377del	ENSP00000501839.1:n.2070-401_2070-377del
ENST00000675404.1:n.2305-401_2305-377del
ENST00000675483.1:n.2198-401_2198-377del
ENST00000675512.1:c.*2072-401_*2072-377del	ENSP00000502630.1:n.*2072-401_*2072-377del
ENST00000675528.1:n.1561-401_1561-377del
ENST00000675817.1:c.2202-401_2202-377del	ENSP00000502422.1:n.2202-401_2202-377del
ENST00000675872.1:n.2430-401_2430-377del
ENST00000675919.1:c.2070-401_2070-377del	ENSP00000501776.1:n.2070-401_2070-377del
ENST00000675959.1:n.2576-401_2576-377del
ENST00000675987.1:c.*43-401_*43-377del	ENSP00000502145.1:n.*43-401_*43-377del
ENST00000676293.1:c.2070-401_2070-377del	ENSP00000502362.1:n.2070-401_2070-377del
ENST00000676295.1:n.483-401_483-377del
ENST00000676426.1:c.*1070-401_*1070-377del	ENSP00000502359.1:n.*1070-401_*1070-377del
ENST00000235329.9:c.2070-401_2070-377del	ENSP00000235329.5:n.2070-401_2070-377del
ENST00000444836.5:c.2070-401_2070-377del	ENSP00000416338.1:n.2070-401_2070-377del
NM_001127660.1:c.2070-401_2070-377del	NP_001121132.1:n.2070-401_2070-377del
NM_014874.3:c.2070-401_2070-377del , LRG_255t1:c.2070-401_2070-377del	NP_055689.1:n.2070-401_2070-377del
XM_005263543.2:c.2070-401_2070-377del	XP_005263600.1:n.2070-401_2070-377del
XM_005263545.2:c.2070-401_2070-377del	XP_005263602.1:n.2070-401_2070-377del
XM_005263547.2:c.2070-401_2070-377del	XP_005263604.1:n.2070-401_2070-377del
XM_005263548.2:c.2070-401_2070-377del	XP_005263605.1:n.2070-401_2070-377del
XM_005263543.3:c.2070-401_2070-377del	XP_005263600.1:n.2070-401_2070-377del
XM_005263545.3:c.2070-401_2070-377del	XP_005263602.1:n.2070-401_2070-377del
XM_005263547.3:c.2070-401_2070-377del	XP_005263604.1:n.2070-401_2070-377del
XM_005263548.3:c.2070-401_2070-377del	XP_005263605.1:n.2070-401_2070-377del
XM_024451299.1:c.2070-401_2070-377del	XP_024307067.1:n.2070-401_2070-377del
NM_014874.4:c.2070-401_2070-377del MANE Select	NP_055689.1:n.2070-401_2070-377del
NM_001127660.2:c.2070-401_2070-377del	NP_001121132.1:n.2070-401_2070-377del