Canonical Allele Identifier: CA1676681717
Gene: SOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159679608A= , CM000668.2:g.159679608A= GRCh38
NC_000006.11:g.160100640A= , CM000668.1:g.160100640A= GRCh37
NC_000006.10:g.160020630A= NCBI36
NG_008729.1:g.18714T=
NG_008729.3:g.87922T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000538183.7:c.*2885T= MANE Select ENSP00000446252.1:n.*2885T=
ENST00000367054.6:c.*20-310T= ENSP00000356021.2:n.*20-310T=
ENST00000367055.8:c.*20-310T= ENSP00000356022.4:n.*20-310T=
ENST00000538183.6:c.*2885T= ENSP00000446252.1:n.*2885T=
ENST00000546087.5:c.*20-310T= ENSP00000442920.1:n.*20-310T=
ENST00000546260.5:c.*3258T= ENSP00000440131.1:n.*3258T=
NM_001024465.1:c.*20-310T= NP_001019636.1:n.*20-310T=
NM_001024466.1:c.*20-310T= NP_001019637.1:n.*20-310T=
NM_000636.3:c.*2885T= NP_000627.2:n.*2885T=
NM_001024465.2:c.*20-310T= NP_001019636.1:n.*20-310T=
NM_001024466.2:c.*20-310T= NP_001019637.1:n.*20-310T=
NM_001322814.1:c.*2885T= NP_001309743.1:n.*2885T=
NM_001322815.1:c.*2885T= NP_001309744.1:n.*2885T=
NM_001322817.1:c.*20-310T= NP_001309746.1:n.*20-310T=
NM_001322819.1:c.*2885T= NP_001309748.1:n.*2885T=
NM_001322820.1:c.*2885T= NP_001309749.1:n.*2885T=
NM_000636.4:c.*2885T= MANE Select NP_000627.2:n.*2885T=
NM_001024465.3:c.*20-310T= NP_001019636.1:n.*20-310T=
NM_001024466.3:c.*20-310T= NP_001019637.1:n.*20-310T=
NM_001322814.2:c.*2885T= NP_001309743.1:n.*2885T=
NM_001322815.2:c.*2885T= NP_001309744.1:n.*2885T=
NM_001322817.2:c.*20-310T= NP_001309746.1:n.*20-310T=
NM_001322819.2:c.*2885T= NP_001309748.1:n.*2885T=
NM_001322820.2:c.*2885T= NP_001309749.1:n.*2885T=