Canonical Allele Identifier: CA1676683376

Gene: SOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.159682052C= , CM000668.2:g.159682052C=	GRCh38
NC_000006.11:g.160103084C= , CM000668.1:g.160103084C=	GRCh37
NC_000006.10:g.160023074C=	NCBI36
NG_008729.1:g.16270G=
NG_008729.3:g.85478G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000538183.7:c.*441G= MANE Select	ENSP00000446252.1:n.*441G=
ENST00000367054.6:c.*19+422G=	ENSP00000356021.2:n.*19+422G=
ENST00000367055.8:c.*19+422G=	ENSP00000356022.4:n.*19+422G=
ENST00000538183.6:c.*441G=	ENSP00000446252.1:n.*441G=
ENST00000546087.5:c.*19+422G=	ENSP00000442920.1:n.*19+422G=
ENST00000546260.5:c.*814G=	ENSP00000440131.1:n.*814G=
NM_000636.2:c.*441G=	NP_000627.2:n.*441G=
NM_001024465.1:c.*19+422G=	NP_001019636.1:n.*19+422G=
NM_001024466.1:c.*19+422G=	NP_001019637.1:n.*19+422G=
NM_000636.3:c.*441G=	NP_000627.2:n.*441G=
NM_001024465.2:c.*19+422G=	NP_001019636.1:n.*19+422G=
NM_001024466.2:c.*19+422G=	NP_001019637.1:n.*19+422G=
NM_001322814.1:c.*441G=	NP_001309743.1:n.*441G=
NM_001322815.1:c.*441G=	NP_001309744.1:n.*441G=
NM_001322817.1:c.*19+422G=	NP_001309746.1:n.*19+422G=
NM_001322819.1:c.*441G=	NP_001309748.1:n.*441G=
NM_001322820.1:c.*441G=	NP_001309749.1:n.*441G=
NM_000636.4:c.*441G= MANE Select	NP_000627.2:n.*441G=
NM_001024465.3:c.*19+422G=	NP_001019636.1:n.*19+422G=
NM_001024466.3:c.*19+422G=	NP_001019637.1:n.*19+422G=
NM_001322814.2:c.*441G=	NP_001309743.1:n.*441G=
NM_001322815.2:c.*441G=	NP_001309744.1:n.*441G=
NM_001322817.2:c.*19+422G=	NP_001309746.1:n.*19+422G=
NM_001322819.2:c.*441G=	NP_001309748.1:n.*441G=
NM_001322820.2:c.*441G=	NP_001309749.1:n.*441G=