Canonical Allele Identifier: CA1676686076

Gene: SOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.159688202C= , CM000668.2:g.159688202C=	GRCh38
NC_000006.11:g.160109234C= , CM000668.1:g.160109234C=	GRCh37
NC_000006.10:g.160029224C=	NCBI36
NG_008729.1:g.10120G=
NG_008729.3:g.79328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000538183.7:c.267G= MANE Select	ENSP00000446252.1:p.Lys89=
ENST00000337404.8:c.227-3169G=	ENSP00000337127.4:n.227-3169G=
ENST00000367054.6:c.227-3169G=	ENSP00000356021.2:n.227-3169G=
ENST00000367055.8:c.267G=	ENSP00000356022.4:p.Lys89=
ENST00000401980.3:c.89-3169G=	ENSP00000384196.3:n.89-3169G=
ENST00000444946.6:c.267G=	ENSP00000404804.2:p.Lys89=
ENST00000535459.5:n.147G=
ENST00000535561.5:c.336G=	ENSP00000445015.1:p.Lys112=
ENST00000537657.5:c.129G=	ENSP00000439191.1:p.Lys43=
ENST00000538183.6:c.267G=	ENSP00000446252.1:p.Lys89=
ENST00000540491.1:n.246-3169G=
ENST00000541573.5:n.160G=
ENST00000545162.5:c.336G=	ENSP00000441362.1:p.Lys112=
ENST00000546087.5:c.129G=	ENSP00000442920.1:p.Lys43=
ENST00000546260.5:c.397G=	ENSP00000440131.1:p.Val133=
NM_000636.2:c.267G=	NP_000627.2:p.Lys89=
NM_001024465.1:c.267G=	NP_001019636.1:p.Lys89=
NM_001024466.1:c.227-3169G=	NP_001019637.1:n.227-3169G=
NM_000636.3:c.267G=	NP_000627.2:p.Lys89=
NM_001024465.2:c.267G=	NP_001019636.1:p.Lys89=
NM_001024466.2:c.227-3169G=	NP_001019637.1:n.227-3169G=
NM_001322814.1:c.227-3169G=	NP_001309743.1:n.227-3169G=
NM_001322815.1:c.267G=	NP_001309744.1:p.Lys89=
NM_001322817.1:c.129G=	NP_001309746.1:p.Lys43=
NM_001322819.1:c.129G=	NP_001309748.1:p.Lys43=
NM_001322820.1:c.129G=	NP_001309749.1:p.Lys43=
NM_000636.4:c.267G= MANE Select	NP_000627.2:p.Lys89=
NM_001024465.3:c.267G=	NP_001019636.1:p.Lys89=
NM_001024466.3:c.227-3169G=	NP_001019637.1:n.227-3169G=
NM_001322814.2:c.227-3169G=	NP_001309743.1:n.227-3169G=
NM_001322815.2:c.267G=	NP_001309744.1:p.Lys89=
NM_001322817.2:c.129G=	NP_001309746.1:p.Lys43=
NM_001322819.2:c.129G=	NP_001309748.1:p.Lys43=
NM_001322820.2:c.129G=	NP_001309749.1:p.Lys43=