Canonical Allele Identifier: CA15110327

Gene: MFN2

Linked Data

• dbSNP Id: rs2336384
• gnomAD v2: 1-12046063-G-T
• gnomAD v3: 1-11986006-G-T
• gnomAD v4: 1-11986006-G-T
• MyVariant Identifiers: chr1:g.12046063G>T (hg19) ; chr1:g.11986006G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11986006G>T , CM000663.2:g.11986006G>T	GRCh38
NC_000001.10:g.12046063G>T , CM000663.1:g.12046063G>T	GRCh37
NC_000001.9:g.11968650G>T	NCBI36
NG_007945.1:g.10826G>T , LRG_255:g.10826G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000235329.10:c.-4-3159G>T MANE Select	ENSP00000235329.5:n.-4-3159G>T
ENST00000412236.2:c.-4-3159G>T	ENSP00000412023.1:n.-4-3159G>T
ENST00000674548.1:c.-94-2421G>T	ENSP00000502185.1:n.-94-2421G>T
ENST00000674658.1:c.-35+3416G>T	ENSP00000502334.1:n.-35+3416G>T
ENST00000674706.1:n.436-3159G>T
ENST00000674817.1:c.-4-3159G>T	ENSP00000502151.1:n.-4-3159G>T
ENST00000674910.1:c.-126-2716G>T	ENSP00000501716.1:n.-126-2716G>T
ENST00000675053.1:c.-4-3159G>T	ENSP00000501646.1:n.-4-3159G>T
ENST00000675113.1:c.-66-2776G>T	ENSP00000502623.1:n.-66-2776G>T
ENST00000675194.1:n.422-3159G>T
ENST00000675231.1:c.-4-3159G>T	ENSP00000502404.1:n.-4-3159G>T
ENST00000675298.1:c.-4-3159G>T	ENSP00000501839.1:n.-4-3159G>T
ENST00000675512.1:c.-4-3159G>T	ENSP00000502630.1:n.-4-3159G>T
ENST00000675530.1:c.-4-3159G>T	ENSP00000501972.1:n.-4-3159G>T
ENST00000675781.1:c.-4-3159G>T	ENSP00000501947.1:n.-4-3159G>T
ENST00000675817.1:c.-4-3159G>T	ENSP00000502422.1:n.-4-3159G>T
ENST00000675872.1:n.248-3159G>T
ENST00000675919.1:c.-94-2421G>T	ENSP00000501776.1:n.-94-2421G>T
ENST00000675959.1:n.394-3159G>T
ENST00000675987.1:c.-4-3159G>T	ENSP00000502145.1:n.-4-3159G>T
ENST00000676293.1:c.-126-2716G>T	ENSP00000502362.1:n.-126-2716G>T
ENST00000676369.1:c.-4-3159G>T	ENSP00000502005.1:n.-4-3159G>T
ENST00000676426.1:c.-4-3159G>T	ENSP00000502359.1:n.-4-3159G>T
ENST00000235329.9:c.-4-3159G>T	ENSP00000235329.5:n.-4-3159G>T
ENST00000412236.1:c.-4-3159G>T	ENSP00000412023.1:n.-4-3159G>T
ENST00000444836.5:c.-4-3159G>T	ENSP00000416338.1:n.-4-3159G>T
ENST00000484391.5:n.116-3159G>T
ENST00000490079.5:n.376-3159G>T
ENST00000497302.1:n.196-3159G>T
NM_001127660.1:c.-4-3159G>T	NP_001121132.1:n.-4-3159G>T
NM_014874.3:c.-4-3159G>T , LRG_255t1:c.-4-3159G>T	NP_055689.1:n.-4-3159G>T
XM_005263543.2:c.-4-3159G>T	XP_005263600.1:n.-4-3159G>T
XM_005263545.2:c.-4-3159G>T	XP_005263602.1:n.-4-3159G>T
XM_005263547.2:c.-4-3159G>T	XP_005263604.1:n.-4-3159G>T
XM_005263548.2:c.-4-3159G>T	XP_005263605.1:n.-4-3159G>T
XM_005263543.3:c.-4-3159G>T	XP_005263600.1:n.-4-3159G>T
XM_005263545.3:c.-4-3159G>T	XP_005263602.1:n.-4-3159G>T
XM_005263547.3:c.-4-3159G>T	XP_005263604.1:n.-4-3159G>T
XM_005263548.3:c.-4-3159G>T	XP_005263605.1:n.-4-3159G>T
XM_024451299.1:c.-4-3159G>T	XP_024307067.1:n.-4-3159G>T
NM_014874.4:c.-4-3159G>T MANE Select	NP_055689.1:n.-4-3159G>T
NM_001127660.2:c.-4-3159G>T	NP_001121132.1:n.-4-3159G>T