Canonical Allele Identifier: CA416363798

Gene: MFN2

Linked Data

• MyVariant Identifiers: chr1:g.12058893G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11998836G>C , CM000663.2:g.11998836G>C	GRCh38
NC_000001.10:g.12058893G>C , CM000663.1:g.12058893G>C	GRCh37
NC_000001.9:g.11981480G>C	NCBI36
NG_007945.1:g.23656G>C , LRG_255:g.23656G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000235329.10:c.666G>C MANE Select	ENSP00000235329.5:p.Val222=
ENST00000674548.1:c.666G>C	ENSP00000502185.1:p.Val222=
ENST00000674658.1:c.321G>C	ENSP00000502334.1:p.Val107=
ENST00000674706.1:n.1105G>C
ENST00000674817.1:c.666G>C	ENSP00000502151.1:p.Val222=
ENST00000674910.1:c.666G>C	ENSP00000501716.1:p.Val222=
ENST00000675053.1:c.666G>C	ENSP00000501646.1:p.Val222=
ENST00000675113.1:c.666G>C	ENSP00000502623.1:p.Val222=
ENST00000675194.1:n.1091G>C
ENST00000675231.1:c.666G>C	ENSP00000502404.1:p.Val222=
ENST00000675298.1:c.666G>C	ENSP00000501839.1:p.Val222=
ENST00000675374.1:n.356G>C
ENST00000675483.1:n.794G>C
ENST00000675512.1:c.*668G>C	ENSP00000502630.1:n.*668G>C
ENST00000675528.1:n.157G>C
ENST00000675817.1:c.666G>C	ENSP00000502422.1:p.Val222=
ENST00000675872.1:n.917G>C
ENST00000675919.1:c.666G>C	ENSP00000501776.1:p.Val222=
ENST00000675959.1:n.1063G>C
ENST00000675987.1:c.666G>C	ENSP00000502145.1:p.Val222=
ENST00000676293.1:c.666G>C	ENSP00000502362.1:p.Val222=
ENST00000676426.1:c.599+1415G>C	ENSP00000502359.1:n.599+1415G>C
ENST00000235329.9:c.666G>C	ENSP00000235329.5:p.Val222=
ENST00000444836.5:c.666G>C	ENSP00000416338.1:p.Val222=
NM_001127660.1:c.666G>C	NP_001121132.1:p.Val222=
NM_014874.3:c.666G>C , LRG_255t1:c.666G>C	NP_055689.1:p.Val222=
XM_005263543.2:c.666G>C	XP_005263600.1:p.Val222=
XM_005263545.2:c.666G>C	XP_005263602.1:p.Val222=
XM_005263547.2:c.666G>C	XP_005263604.1:p.Val222=
XM_005263548.2:c.666G>C	XP_005263605.1:p.Val222=
XM_005263543.3:c.666G>C	XP_005263600.1:p.Val222=
XM_005263545.3:c.666G>C	XP_005263602.1:p.Val222=
XM_005263547.3:c.666G>C	XP_005263604.1:p.Val222=
XM_005263548.3:c.666G>C	XP_005263605.1:p.Val222=
XM_024451299.1:c.666G>C	XP_024307067.1:p.Val222=
NM_014874.4:c.666G>C MANE Select	NP_055689.1:p.Val222=
NM_001127660.2:c.666G>C	NP_001121132.1:p.Val222=