Canonical Allele Identifier: CA410035915
Gene: SOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.33032111A>C (hg19) chr21:g.31659798A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31659798A>C , CM000683.2:g.31659798A>C GRCh38
NC_000021.8:g.33032111A>C , CM000683.1:g.33032111A>C GRCh37
NC_000021.7:g.31953982A>C NCBI36
NG_008689.1:g.5177A>C , LRG_652:g.5177A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270142.11:c.29A>C MANE Select ENSP00000270142.7:p.Lys10Thr
ENST00000270142.10:c.29A>C ENSP00000270142.6:p.Lys10Thr
ENST00000389995.4:c.15+14A>C ENSP00000374645.4:n.15+14A>C
ENST00000470944.1:n.90A>C
ENST00000476106.5:n.106A>C
NM_000454.4:c.29A>C , LRG_652t1:c.29A>C NP_000445.1:p.Lys10Thr
NM_000454.5:c.29A>C MANE Select NP_000445.1:p.Lys10Thr
Search 100 bp 5'
Search 100 bp 3'