Canonical Allele Identifier: CA1676708872
Gene: SOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159692843G= , CM000668.2:g.159692843G= GRCh38
NC_000006.11:g.160113875G= , CM000668.1:g.160113875G= GRCh37
NC_000006.10:g.160033865G= NCBI36
NG_008729.1:g.5479C=
NG_008729.3:g.74687C=

Transcript Alleles

HGVS Amino-acid change
ENST00000538183.7:c.44C= MANE Select ENSP00000446252.1:p.Pro15=
ENST00000337404.8:c.44C= ENSP00000337127.4:p.Pro15=
ENST00000367054.6:c.44C= ENSP00000356021.2:p.Pro15=
ENST00000367055.8:c.44C= ENSP00000356022.4:p.Pro15=
ENST00000401980.3:c.-95C= ENSP00000384196.3:n.-95C=
ENST00000444946.6:c.44C= ENSP00000404804.2:p.Pro15=
ENST00000452684.2:c.44C= ENSP00000406713.2:p.Pro15=
ENST00000535561.5:c.113C= ENSP00000445015.1:p.Pro38=
ENST00000537657.5:c.-95C= ENSP00000439191.1:n.-95C=
ENST00000538183.6:c.44C= ENSP00000446252.1:p.Pro15=
ENST00000545162.5:c.113C= ENSP00000441362.1:p.Pro38=
ENST00000546087.5:c.-95C= ENSP00000442920.1:n.-95C=
ENST00000546260.5:c.44C= ENSP00000440131.1:p.Pro15=
NM_000636.2:c.44C= NP_000627.2:p.Pro15=
NM_001024465.1:c.44C= NP_001019636.1:p.Pro15=
NM_001024466.1:c.44C= NP_001019637.1:p.Pro15=
NM_000636.3:c.44C= NP_000627.2:p.Pro15=
NM_001024465.2:c.44C= NP_001019636.1:p.Pro15=
NM_001024466.2:c.44C= NP_001019637.1:p.Pro15=
NM_001322814.1:c.44C= NP_001309743.1:p.Pro15=
NM_001322815.1:c.44C= NP_001309744.1:p.Pro15=
NM_001322816.1:c.44C= NP_001309745.1:p.Pro15=
NM_001322817.1:c.-95C= NP_001309746.1:n.-95C=
NM_001322819.1:c.-95C= NP_001309748.1:n.-95C=
NM_001322820.1:c.-95C= NP_001309749.1:n.-95C=
NM_000636.4:c.44C= MANE Select NP_000627.2:p.Pro15=
NM_001024465.3:c.44C= NP_001019636.1:p.Pro15=
NM_001024466.3:c.44C= NP_001019637.1:p.Pro15=
NM_001322814.2:c.44C= NP_001309743.1:p.Pro15=
NM_001322815.2:c.44C= NP_001309744.1:p.Pro15=
NM_001322817.2:c.-95C= NP_001309746.1:n.-95C=
NM_001322819.2:c.-95C= NP_001309748.1:n.-95C=
NM_001322820.2:c.-95C= NP_001309749.1:n.-95C=
NM_001322816.2:c.44C= NP_001309745.1:p.Pro15=