Canonical Allele Identifier: CA116469
Gene: SUOX HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 3820
dbSNP Id: rs121908007

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56004039G>A , CM000674.2:g.56004039G>A GRCh38
NC_000012.11:g.56397823G>A , CM000674.1:g.56397823G>A GRCh37
NC_000012.10:g.54684090G>A NCBI36
NG_008136.1:g.11781G>A

Transcript Alleles

HGVS Amino-acid change
NM_000456.2:c.650G>A VV NP_000447.2:p.Arg217Gln
NM_001032386.1:c.650G>A VV NP_001027558.1:p.Arg217Gln
NM_001032387.1:c.650G>A VV NP_001027559.1:p.Arg217Gln
XM_005269112.1:c.671G>A XP_005269169.1:p.Arg224Gln
XM_017019905.2:c.671G>A XP_016875394.1:p.Arg224Gln
XM_017019906.1:c.671G>A XP_016875395.1:p.Arg224Gln
XM_017019907.2:c.650G>A XP_016875396.1:p.Arg217Gln
XM_017019908.1:c.650G>A XP_016875397.1:p.Arg217Gln
XM_024449167.1:c.671G>A XP_024304935.1:p.Arg224Gln
NM_001032386.2:c.650G>A VV MANE Preferred NP_001027558.1:p.Arg217Gln
ENST00000266971.7:c.650G>A ENSP00000266971.3:p.Arg217Gln
ENST00000356124.8:c.650G>A ENSP00000348440.4:p.Arg217Gln
ENST00000394109.7:c.650G>A ENSP00000377668.3:p.Arg217Gln
ENST00000394115.6:c.650G>A ENSP00000377674.2:p.Arg217Gln
ENST00000548274.5:c.650G>A ENSP00000450245.1:p.Arg217Gln
ENST00000550065.1:c.650G>A ENSP00000450264.1:p.Arg217Gln
ENST00000550340.5:n.535G>A
ENST00000551841.6:c.268-115G>A ENSP00000449443.1:p.=