Canonical Allele Identifier: CA1676686056

Gene: SOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.159688139A= , CM000668.2:g.159688139A=	GRCh38
NC_000006.11:g.160109171A= , CM000668.1:g.160109171A=	GRCh37
NC_000006.10:g.160029161A=	NCBI36
NG_008729.1:g.10183T=
NG_008729.3:g.79391T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000538183.7:c.330T= MANE Select	ENSP00000446252.1:p.Gly110=
ENST00000337404.8:c.227-3106T=	ENSP00000337127.4:n.227-3106T=
ENST00000367054.6:c.227-3106T=	ENSP00000356021.2:n.227-3106T=
ENST00000367055.8:c.330T=	ENSP00000356022.4:p.Gly110=
ENST00000401980.3:c.89-3106T=	ENSP00000384196.3:n.89-3106T=
ENST00000444946.6:c.330T=	ENSP00000404804.2:p.Gly110=
ENST00000535459.5:n.210T=
ENST00000535561.5:c.399T=	ENSP00000445015.1:p.Gly133=
ENST00000537657.5:c.192T=	ENSP00000439191.1:p.Gly64=
ENST00000538183.6:c.330T=	ENSP00000446252.1:p.Gly110=
ENST00000540491.1:n.246-3106T=
ENST00000541573.5:n.223T=
ENST00000545162.5:c.399T=	ENSP00000441362.1:p.Gly133=
ENST00000546087.5:c.192T=	ENSP00000442920.1:p.Gly64=
ENST00000546260.5:c.*34T=	ENSP00000440131.1:n.*34T=
NM_000636.2:c.330T=	NP_000627.2:p.Gly110=
NM_001024465.1:c.330T=	NP_001019636.1:p.Gly110=
NM_001024466.1:c.227-3106T=	NP_001019637.1:n.227-3106T=
NM_000636.3:c.330T=	NP_000627.2:p.Gly110=
NM_001024465.2:c.330T=	NP_001019636.1:p.Gly110=
NM_001024466.2:c.227-3106T=	NP_001019637.1:n.227-3106T=
NM_001322814.1:c.227-3106T=	NP_001309743.1:n.227-3106T=
NM_001322815.1:c.330T=	NP_001309744.1:p.Gly110=
NM_001322817.1:c.192T=	NP_001309746.1:p.Gly64=
NM_001322819.1:c.192T=	NP_001309748.1:p.Gly64=
NM_001322820.1:c.192T=	NP_001309749.1:p.Gly64=
NM_000636.4:c.330T= MANE Select	NP_000627.2:p.Gly110=
NM_001024465.3:c.330T=	NP_001019636.1:p.Gly110=
NM_001024466.3:c.227-3106T=	NP_001019637.1:n.227-3106T=
NM_001322814.2:c.227-3106T=	NP_001309743.1:n.227-3106T=
NM_001322815.2:c.330T=	NP_001309744.1:p.Gly110=
NM_001322817.2:c.192T=	NP_001309746.1:p.Gly64=
NM_001322819.2:c.192T=	NP_001309748.1:p.Gly64=
NM_001322820.2:c.192T=	NP_001309749.1:p.Gly64=