Canonical Allele Identifier: CA1676708811

Gene: SOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.159692742G= , CM000668.2:g.159692742G=	GRCh38
NC_000006.11:g.160113774G= , CM000668.1:g.160113774G=	GRCh37
NC_000006.10:g.160033764G=	NCBI36
NG_008729.1:g.5580C=
NG_008729.3:g.74788C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000538183.7:c.145C= MANE Select	ENSP00000446252.1:p.Leu49=
ENST00000337404.8:c.145C=	ENSP00000337127.4:p.Leu49=
ENST00000367054.6:c.145C=	ENSP00000356021.2:p.Leu49=
ENST00000367055.8:c.145C=	ENSP00000356022.4:p.Leu49=
ENST00000401980.3:c.7C=	ENSP00000384196.3:p.Leu3=
ENST00000444946.6:c.145C=	ENSP00000404804.2:p.Leu49=
ENST00000452684.2:c.145C=	ENSP00000406713.2:p.Leu49=
ENST00000535561.5:c.214C=	ENSP00000445015.1:p.Leu72=
ENST00000537657.5:c.7C=	ENSP00000439191.1:p.Leu3=
ENST00000538183.6:c.145C=	ENSP00000446252.1:p.Leu49=
ENST00000545162.5:c.214C=	ENSP00000441362.1:p.Leu72=
ENST00000546087.5:c.7C=	ENSP00000442920.1:p.Leu3=
ENST00000546260.5:c.145C=	ENSP00000440131.1:p.Leu49=
NM_000636.2:c.145C=	NP_000627.2:p.Leu49=
NM_001024465.1:c.145C=	NP_001019636.1:p.Leu49=
NM_001024466.1:c.145C=	NP_001019637.1:p.Leu49=
NM_000636.3:c.145C=	NP_000627.2:p.Leu49=
NM_001024465.2:c.145C=	NP_001019636.1:p.Leu49=
NM_001024466.2:c.145C=	NP_001019637.1:p.Leu49=
NM_001322814.1:c.145C=	NP_001309743.1:p.Leu49=
NM_001322815.1:c.145C=	NP_001309744.1:p.Leu49=
NM_001322816.1:c.145C=	NP_001309745.1:p.Leu49=
NM_001322817.1:c.7C=	NP_001309746.1:p.Leu3=
NM_001322819.1:c.7C=	NP_001309748.1:p.Leu3=
NM_001322820.1:c.7C=	NP_001309749.1:p.Leu3=
NM_000636.4:c.145C= MANE Select	NP_000627.2:p.Leu49=
NM_001024465.3:c.145C=	NP_001019636.1:p.Leu49=
NM_001024466.3:c.145C=	NP_001019637.1:p.Leu49=
NM_001322814.2:c.145C=	NP_001309743.1:p.Leu49=
NM_001322815.2:c.145C=	NP_001309744.1:p.Leu49=
NM_001322817.2:c.7C=	NP_001309746.1:p.Leu3=
NM_001322819.2:c.7C=	NP_001309748.1:p.Leu3=
NM_001322820.2:c.7C=	NP_001309749.1:p.Leu3=
NM_001322816.2:c.145C=	NP_001309745.1:p.Leu49=