Canonical Allele Identifier: CA1153896854

Gene: MFN2

Linked Data

• dbSNP Id: rs1158242896
• gnomAD v4: 1-11980292-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980292G>T , CM000663.2:g.11980292G>T	GRCh38
NC_000001.10:g.12040349G>T , CM000663.1:g.12040349G>T	GRCh37
NC_000001.9:g.11962936G>T	NCBI36
NG_007945.1:g.5112G>T , LRG_255:g.5112G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-406G>T	ENSP00000412023.1:n.-406G>T
ENST00000674548.1:c.-287G>T	ENSP00000502185.1:n.-287G>T
ENST00000674658.1:c.-440G>T	ENSP00000502334.1:n.-440G>T
ENST00000674706.1:n.34G>T
ENST00000674817.1:c.-197G>T	ENSP00000502151.1:n.-197G>T
ENST00000674910.1:c.-319G>T	ENSP00000501716.1:n.-319G>T
ENST00000675053.1:c.-245G>T	ENSP00000501646.1:n.-245G>T
ENST00000675194.1:n.84G>T
ENST00000675298.1:c.-342G>T	ENSP00000501839.1:n.-342G>T
ENST00000675530.1:c.-338G>T	ENSP00000501972.1:n.-338G>T
ENST00000675817.1:c.-342G>T	ENSP00000502422.1:n.-342G>T
ENST00000675872.1:n.55G>T
ENST00000675959.1:n.56G>T
ENST00000676369.1:c.-410G>T	ENSP00000502005.1:n.-410G>T
ENST00000676426.1:c.-342G>T	ENSP00000502359.1:n.-342G>T
ENST00000444836.5:c.-197G>T	ENSP00000416338.1:n.-197G>T
NM_001127660.1:c.-197G>T	NP_001121132.1:n.-197G>T
NM_014874.3:c.-342G>T , LRG_255t1:c.-342G>T	NP_055689.1:n.-342G>T
XM_005263543.2:c.-410G>T	XP_005263600.1:n.-410G>T
XM_005263548.2:c.-406G>T	XP_005263605.1:n.-406G>T
XM_005263543.3:c.-410G>T	XP_005263600.1:n.-410G>T
XM_005263548.3:c.-406G>T	XP_005263605.1:n.-406G>T