Canonical Allele Identifier: CA366293943

Gene: SOD2

Linked Data

• MyVariant Identifiers: chr6:g.160109217T>G (hg19) ; chr6:g.159688185T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.159688185T>G , CM000668.2:g.159688185T>G	GRCh38
NC_000006.11:g.160109217T>G , CM000668.1:g.160109217T>G	GRCh37
NC_000006.10:g.160029207T>G	NCBI36
NG_008729.1:g.10137A>C
NG_008729.3:g.79345A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000538183.7:c.284A>C MANE Select	ENSP00000446252.1:p.His95Pro
ENST00000337404.8:c.227-3152A>C	ENSP00000337127.4:n.227-3152A>C
ENST00000367054.6:c.227-3152A>C	ENSP00000356021.2:n.227-3152A>C
ENST00000367055.8:c.284A>C	ENSP00000356022.4:p.His95Pro
ENST00000401980.3:c.89-3152A>C	ENSP00000384196.3:n.89-3152A>C
ENST00000444946.6:c.284A>C	ENSP00000404804.2:p.His95Pro
ENST00000535459.5:n.164A>C
ENST00000535561.5:c.353A>C	ENSP00000445015.1:p.His118Pro
ENST00000537657.5:c.146A>C	ENSP00000439191.1:p.His49Pro
ENST00000538183.6:c.284A>C	ENSP00000446252.1:p.His95Pro
ENST00000540491.1:n.246-3152A>C
ENST00000541573.5:n.177A>C
ENST00000545162.5:c.353A>C	ENSP00000441362.1:p.His118Pro
ENST00000546087.5:c.146A>C	ENSP00000442920.1:p.His49Pro
ENST00000546260.5:c.414A>C	ENSP00000440131.1:p.Ser138=
NM_000636.2:c.284A>C	NP_000627.2:p.His95Pro
NM_001024465.1:c.284A>C	NP_001019636.1:p.His95Pro
NM_001024466.1:c.227-3152A>C	NP_001019637.1:n.227-3152A>C
NM_000636.3:c.284A>C	NP_000627.2:p.His95Pro
NM_001024465.2:c.284A>C	NP_001019636.1:p.His95Pro
NM_001024466.2:c.227-3152A>C	NP_001019637.1:n.227-3152A>C
NM_001322814.1:c.227-3152A>C	NP_001309743.1:n.227-3152A>C
NM_001322815.1:c.284A>C	NP_001309744.1:p.His95Pro
NM_001322817.1:c.146A>C	NP_001309746.1:p.His49Pro
NM_001322819.1:c.146A>C	NP_001309748.1:p.His49Pro
NM_001322820.1:c.146A>C	NP_001309749.1:p.His49Pro
NM_000636.4:c.284A>C MANE Select	NP_000627.2:p.His95Pro
NM_001024465.3:c.284A>C	NP_001019636.1:p.His95Pro
NM_001024466.3:c.227-3152A>C	NP_001019637.1:n.227-3152A>C
NM_001322814.2:c.227-3152A>C	NP_001309743.1:n.227-3152A>C
NM_001322815.2:c.284A>C	NP_001309744.1:p.His95Pro
NM_001322817.2:c.146A>C	NP_001309746.1:p.His49Pro
NM_001322819.2:c.146A>C	NP_001309748.1:p.His49Pro
NM_001322820.2:c.146A>C	NP_001309749.1:p.His49Pro