Canonical Allele Identifier: CA410037531
Gene: SOD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 695024
dbSNP Id: rs1378590183

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31667335C>T , CM000683.2:g.31667335C>T GRCh38
NC_000021.8:g.33039648C>T , CM000683.1:g.33039648C>T GRCh37
NC_000021.7:g.31961519C>T NCBI36
NG_008689.1:g.12714C>T , LRG_652:g.12714C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000270142.11:c.317C>T MANE Select ENSP00000270142.7:p.Ser106Leu
ENST00000270142.10:c.317C>T ENSP00000270142.6:p.Ser106Leu
ENST00000389995.4:c.260C>T ENSP00000374645.4:p.Ser87Leu
ENST00000470944.1:n.1245C>T
ENST00000476106.5:n.580C>T
NM_000454.4:c.317C>T , LRG_652t1:c.317C>T NP_000445.1:p.Ser106Leu
NM_000454.5:c.317C>T MANE Select NP_000445.1:p.Ser106Leu