Canonical Allele Identifier: CA124296
Gene: SOD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14766
dbSNP Id: rs80265967

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31667290A>C , CM000683.2:g.31667290A>C GRCh38
NC_000021.8:g.33039603A>C , CM000683.1:g.33039603A>C GRCh37
NC_000021.7:g.31961474A>C NCBI36
NG_008689.1:g.12669A>C , LRG_652:g.12669A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270142.11:c.272A>C MANE Select ENSP00000270142.7:p.Asp91Ala
ENST00000270142.10:c.272A>C ENSP00000270142.6:p.Asp91Ala
ENST00000389995.4:c.215A>C ENSP00000374645.4:p.Asp72Ala
ENST00000470944.1:n.1200A>C
ENST00000476106.5:n.535A>C
NM_000454.4:c.272A>C , LRG_652t1:c.272A>C NP_000445.1:p.Asp91Ala
NM_000454.5:c.272A>C MANE Select NP_000445.1:p.Asp91Ala