Canonical Allele Identifier: CA2574216582

Gene: MFN2

Linked Data

• gnomAD v4: 1-12001921-TGGCCCTTGGTTGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12001927_12001940del , CM000663.2:g.12001927_12001940del	GRCh38
NC_000001.10:g.12061984_12061997del , CM000663.1:g.12061984_12061997del	GRCh37
NC_000001.9:g.11984571_11984584del	NCBI36
NG_007945.1:g.26747_26760del , LRG_255:g.26747_26760del

Transcript Alleles

HGVS	Amino-acid change
ENST00000235329.10:c.1039-55_1039-42del MANE Select	ENSP00000235329.5:n.1039-55_1039-42del
ENST00000674548.1:c.1039-55_1039-42del	ENSP00000502185.1:n.1039-55_1039-42del
ENST00000674658.1:c.694-55_694-42del	ENSP00000502334.1:n.694-55_694-42del
ENST00000674817.1:c.1039-55_1039-42del	ENSP00000502151.1:n.1039-55_1039-42del
ENST00000674910.1:c.1039-55_1039-42del	ENSP00000501716.1:n.1039-55_1039-42del
ENST00000675053.1:c.1039-55_1039-42del	ENSP00000501646.1:n.1039-55_1039-42del
ENST00000675113.1:c.1039-55_1039-42del	ENSP00000502623.1:n.1039-55_1039-42del
ENST00000675194.1:n.1464-55_1464-42del
ENST00000675231.1:c.1039-55_1039-42del	ENSP00000502404.1:n.1039-55_1039-42del
ENST00000675298.1:c.1039-55_1039-42del	ENSP00000501839.1:n.1039-55_1039-42del
ENST00000675404.1:n.1274-55_1274-42del
ENST00000675483.1:n.1167-55_1167-42del
ENST00000675512.1:c.*1041-55_*1041-42del	ENSP00000502630.1:n.*1041-55_*1041-42del
ENST00000675528.1:n.530-55_530-42del
ENST00000675817.1:c.1039-55_1039-42del	ENSP00000502422.1:n.1039-55_1039-42del
ENST00000675872.1:n.1399-55_1399-42del
ENST00000675919.1:c.1039-55_1039-42del	ENSP00000501776.1:n.1039-55_1039-42del
ENST00000675959.1:n.1545-55_1545-42del
ENST00000675987.1:c.1039-55_1039-42del	ENSP00000502145.1:n.1039-55_1039-42del
ENST00000676293.1:c.1039-55_1039-42del	ENSP00000502362.1:n.1039-55_1039-42del
ENST00000676426.1:c.*39-55_*39-42del	ENSP00000502359.1:n.*39-55_*39-42del
ENST00000235329.9:c.1039-55_1039-42del	ENSP00000235329.5:n.1039-55_1039-42del
ENST00000444836.5:c.1039-55_1039-42del	ENSP00000416338.1:n.1039-55_1039-42del
NM_001127660.1:c.1039-55_1039-42del	NP_001121132.1:n.1039-55_1039-42del
NM_014874.3:c.1039-55_1039-42del , LRG_255t1:c.1039-55_1039-42del	NP_055689.1:n.1039-55_1039-42del
XM_005263543.2:c.1039-55_1039-42del	XP_005263600.1:n.1039-55_1039-42del
XM_005263545.2:c.1039-55_1039-42del	XP_005263602.1:n.1039-55_1039-42del
XM_005263547.2:c.1039-55_1039-42del	XP_005263604.1:n.1039-55_1039-42del
XM_005263548.2:c.1039-55_1039-42del	XP_005263605.1:n.1039-55_1039-42del
XM_005263543.3:c.1039-55_1039-42del	XP_005263600.1:n.1039-55_1039-42del
XM_005263545.3:c.1039-55_1039-42del	XP_005263602.1:n.1039-55_1039-42del
XM_005263547.3:c.1039-55_1039-42del	XP_005263604.1:n.1039-55_1039-42del
XM_005263548.3:c.1039-55_1039-42del	XP_005263605.1:n.1039-55_1039-42del
XM_024451299.1:c.1039-55_1039-42del	XP_024307067.1:n.1039-55_1039-42del
NM_014874.4:c.1039-55_1039-42del MANE Select	NP_055689.1:n.1039-55_1039-42del
NM_001127660.2:c.1039-55_1039-42del	NP_001121132.1:n.1039-55_1039-42del