Canonical Allele Identifier: CA2680993627

Gene: SOD2

Linked Data

• gnomAD v4: 6-159688024-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.159688026_159688027del , CM000668.2:g.159688026_159688027del	GRCh38
NC_000006.11:g.160109058_160109059del , CM000668.1:g.160109058_160109059del	GRCh37
NC_000006.10:g.160029048_160029049del	NCBI36
NG_008729.1:g.10296_10297del
NG_008729.3:g.79504_79505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000538183.7:c.343+100_343+101del MANE Select	ENSP00000446252.1:n.343+100_343+101del
ENST00000337404.8:c.227-2993_227-2992del	ENSP00000337127.4:n.227-2993_227-2992del
ENST00000367054.6:c.227-2993_227-2992del	ENSP00000356021.2:n.227-2993_227-2992del
ENST00000367055.8:c.343+100_343+101del	ENSP00000356022.4:n.343+100_343+101del
ENST00000401980.3:c.89-2993_89-2992del	ENSP00000384196.3:n.89-2993_89-2992del
ENST00000444946.6:c.343+100_343+101del	ENSP00000404804.2:n.343+100_343+101del
ENST00000535459.5:n.223+100_223+101del
ENST00000535561.5:c.412+100_412+101del	ENSP00000445015.1:n.412+100_412+101del
ENST00000537657.5:c.205+100_205+101del	ENSP00000439191.1:n.205+100_205+101del
ENST00000538183.6:c.343+100_343+101del	ENSP00000446252.1:n.343+100_343+101del
ENST00000540491.1:n.246-2993_246-2992del
ENST00000541573.5:n.236+100_236+101del
ENST00000545162.5:c.412+100_412+101del	ENSP00000441362.1:n.412+100_412+101del
ENST00000546087.5:c.205+100_205+101del	ENSP00000442920.1:n.205+100_205+101del
ENST00000546260.5:c.*47+100_*47+101del	ENSP00000440131.1:n.*47+100_*47+101del
NM_000636.2:c.343+100_343+101del	NP_000627.2:n.343+100_343+101del
NM_001024465.1:c.343+100_343+101del	NP_001019636.1:n.343+100_343+101del
NM_001024466.1:c.227-2993_227-2992del	NP_001019637.1:n.227-2993_227-2992del
NM_000636.3:c.343+100_343+101del	NP_000627.2:n.343+100_343+101del
NM_001024465.2:c.343+100_343+101del	NP_001019636.1:n.343+100_343+101del
NM_001024466.2:c.227-2993_227-2992del	NP_001019637.1:n.227-2993_227-2992del
NM_001322814.1:c.227-2993_227-2992del	NP_001309743.1:n.227-2993_227-2992del
NM_001322815.1:c.343+100_343+101del	NP_001309744.1:n.343+100_343+101del
NM_001322817.1:c.205+100_205+101del	NP_001309746.1:n.205+100_205+101del
NM_001322819.1:c.205+100_205+101del	NP_001309748.1:n.205+100_205+101del
NM_001322820.1:c.205+100_205+101del	NP_001309749.1:n.205+100_205+101del
NM_000636.4:c.343+100_343+101del MANE Select	NP_000627.2:n.343+100_343+101del
NM_001024465.3:c.343+100_343+101del	NP_001019636.1:n.343+100_343+101del
NM_001024466.3:c.227-2993_227-2992del	NP_001019637.1:n.227-2993_227-2992del
NM_001322814.2:c.227-2993_227-2992del	NP_001309743.1:n.227-2993_227-2992del
NM_001322815.2:c.343+100_343+101del	NP_001309744.1:n.343+100_343+101del
NM_001322817.2:c.205+100_205+101del	NP_001309746.1:n.205+100_205+101del
NM_001322819.2:c.205+100_205+101del	NP_001309748.1:n.205+100_205+101del
NM_001322820.2:c.205+100_205+101del	NP_001309749.1:n.205+100_205+101del