Canonical Allele Identifier: CA338438589

Gene: MFN2

Linked Data

• ClinVar Variation Id: 978264
• ClinVar RCV Id: RCV001256669
• dbSNP Id: rs1639047697
• MyVariant Identifiers: chr1:g.12058928T>A (hg19) ; chr1:g.11998871T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11998871T>A , CM000663.2:g.11998871T>A	GRCh38
NC_000001.10:g.12058928T>A , CM000663.1:g.12058928T>A	GRCh37
NC_000001.9:g.11981515T>A	NCBI36
NG_007945.1:g.23691T>A , LRG_255:g.23691T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000235329.10:c.701T>A MANE Select	ENSP00000235329.5:p.Met234Lys
ENST00000674548.1:c.701T>A	ENSP00000502185.1:p.Met234Lys
ENST00000674658.1:c.356T>A	ENSP00000502334.1:p.Met119Lys
ENST00000674706.1:n.1140T>A
ENST00000674817.1:c.701T>A	ENSP00000502151.1:p.Met234Lys
ENST00000674910.1:c.701T>A	ENSP00000501716.1:p.Met234Lys
ENST00000675053.1:c.701T>A	ENSP00000501646.1:p.Met234Lys
ENST00000675113.1:c.701T>A	ENSP00000502623.1:p.Met234Lys
ENST00000675194.1:n.1126T>A
ENST00000675231.1:c.701T>A	ENSP00000502404.1:p.Met234Lys
ENST00000675298.1:c.701T>A	ENSP00000501839.1:p.Met234Lys
ENST00000675374.1:n.391T>A
ENST00000675483.1:n.829T>A
ENST00000675512.1:c.*703T>A	ENSP00000502630.1:n.*703T>A
ENST00000675528.1:n.192T>A
ENST00000675817.1:c.701T>A	ENSP00000502422.1:p.Met234Lys
ENST00000675872.1:n.952T>A
ENST00000675919.1:c.701T>A	ENSP00000501776.1:p.Met234Lys
ENST00000675959.1:n.1098T>A
ENST00000675987.1:c.701T>A	ENSP00000502145.1:p.Met234Lys
ENST00000676293.1:c.701T>A	ENSP00000502362.1:p.Met234Lys
ENST00000676426.1:c.599+1450T>A	ENSP00000502359.1:n.599+1450T>A
ENST00000235329.9:c.701T>A	ENSP00000235329.5:p.Met234Lys
ENST00000444836.5:c.701T>A	ENSP00000416338.1:p.Met234Lys
NM_001127660.1:c.701T>A	NP_001121132.1:p.Met234Lys
NM_014874.3:c.701T>A , LRG_255t1:c.701T>A	NP_055689.1:p.Met234Lys
XM_005263543.2:c.701T>A	XP_005263600.1:p.Met234Lys
XM_005263545.2:c.701T>A	XP_005263602.1:p.Met234Lys
XM_005263547.2:c.701T>A	XP_005263604.1:p.Met234Lys
XM_005263548.2:c.701T>A	XP_005263605.1:p.Met234Lys
XM_005263543.3:c.701T>A	XP_005263600.1:p.Met234Lys
XM_005263545.3:c.701T>A	XP_005263602.1:p.Met234Lys
XM_005263547.3:c.701T>A	XP_005263604.1:p.Met234Lys
XM_005263548.3:c.701T>A	XP_005263605.1:p.Met234Lys
XM_024451299.1:c.701T>A	XP_024307067.1:p.Met234Lys
NM_014874.4:c.701T>A MANE Select	NP_055689.1:p.Met234Lys
NM_001127660.2:c.701T>A	NP_001121132.1:p.Met234Lys