Canonical Allele Identifier: CA338452999

Gene: MFN2

Linked Data

• MyVariant Identifiers: chr1:g.12069671C>G (hg19) ; chr1:g.12009614C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12009614C>G , CM000663.2:g.12009614C>G	GRCh38
NC_000001.10:g.12069671C>G , CM000663.1:g.12069671C>G	GRCh37
NC_000001.9:g.11992258C>G	NCBI36
NG_007945.1:g.34434C>G , LRG_255:g.34434C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235329.10:c.2092C>G MANE Select	ENSP00000235329.5:p.His698Asp
ENST00000674548.1:c.2092C>G	ENSP00000502185.1:p.His698Asp
ENST00000674658.1:c.1747C>G	ENSP00000502334.1:p.His583Asp
ENST00000674817.1:c.2092C>G	ENSP00000502151.1:p.His698Asp
ENST00000674910.1:c.2092C>G	ENSP00000501716.1:p.His698Asp
ENST00000675043.1:n.60C>G
ENST00000675053.1:c.2092C>G	ENSP00000501646.1:p.His698Asp
ENST00000675113.1:c.2092C>G	ENSP00000502623.1:p.His698Asp
ENST00000675231.1:c.2092C>G	ENSP00000502404.1:p.His698Asp
ENST00000675298.1:c.2092C>G	ENSP00000501839.1:p.His698Asp
ENST00000675404.1:n.2327C>G
ENST00000675483.1:n.2220C>G
ENST00000675512.1:c.*2094C>G	ENSP00000502630.1:n.*2094C>G
ENST00000675528.1:n.1583C>G
ENST00000675817.1:c.2224C>G	ENSP00000502422.1:p.His742Asp
ENST00000675872.1:n.2452C>G
ENST00000675919.1:c.2092C>G	ENSP00000501776.1:p.His698Asp
ENST00000675959.1:n.2598C>G
ENST00000675987.1:c.*65C>G	ENSP00000502145.1:n.*65C>G
ENST00000676293.1:c.2092C>G	ENSP00000502362.1:p.His698Asp
ENST00000676295.1:n.505C>G
ENST00000676426.1:c.*1092C>G	ENSP00000502359.1:n.*1092C>G
ENST00000235329.9:c.2092C>G	ENSP00000235329.5:p.His698Asp
ENST00000444836.5:c.2092C>G	ENSP00000416338.1:p.His698Asp
NM_001127660.1:c.2092C>G	NP_001121132.1:p.His698Asp
NM_014874.3:c.2092C>G , LRG_255t1:c.2092C>G	NP_055689.1:p.His698Asp
XM_005263543.2:c.2092C>G	XP_005263600.1:p.His698Asp
XM_005263545.2:c.2092C>G	XP_005263602.1:p.His698Asp
XM_005263547.2:c.2092C>G	XP_005263604.1:p.His698Asp
XM_005263548.2:c.2092C>G	XP_005263605.1:p.His698Asp
XM_005263543.3:c.2092C>G	XP_005263600.1:p.His698Asp
XM_005263545.3:c.2092C>G	XP_005263602.1:p.His698Asp
XM_005263547.3:c.2092C>G	XP_005263604.1:p.His698Asp
XM_005263548.3:c.2092C>G	XP_005263605.1:p.His698Asp
XM_024451299.1:c.2092C>G	XP_024307067.1:p.His698Asp
NM_014874.4:c.2092C>G MANE Select	NP_055689.1:p.His698Asp
NM_001127660.2:c.2092C>G	NP_001121132.1:p.His698Asp