Canonical Allele Identifier: CA237605366
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1045213
ClinVar RCV Id: RCV002254636
dbSNP Id: rs980891298

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56004962A>G , CM000674.2:g.56004962A>G GRCh38
NC_000012.11:g.56398746A>G , CM000674.1:g.56398746A>G GRCh37
NC_000012.10:g.54685013A>G NCBI36
NG_008136.1:g.12704A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266971.8:c.1573A>G MANE Select ENSP00000266971.3:p.Ile525Val
ENST00000266971.7:c.1573A>G ENSP00000266971.3:p.Ile525Val
ENST00000356124.8:c.1573A>G ENSP00000348440.4:p.Ile525Val
ENST00000394109.7:c.1573A>G ENSP00000377668.3:p.Ile525Val
ENST00000394115.6:c.1573A>G ENSP00000377674.2:p.Ile525Val
ENST00000548274.5:c.1573A>G ENSP00000450245.1:p.Ile525Val
ENST00000550065.1:c.1573A>G ENSP00000450264.1:p.Ile525Val
NM_000456.2:c.1573A>G NP_000447.2:p.Ile525Val
NM_001032386.1:c.1573A>G NP_001027558.1:p.Ile525Val
NM_001032387.1:c.1573A>G NP_001027559.1:p.Ile525Val
XM_005269112.1:c.1594A>G XP_005269169.1:p.Ile532Val
XM_017019905.2:c.1594A>G XP_016875394.1:p.Ile532Val
XM_017019906.1:c.1594A>G XP_016875395.1:p.Ile532Val
XM_017019907.2:c.1573A>G XP_016875396.1:p.Ile525Val
XM_017019908.1:c.1573A>G XP_016875397.1:p.Ile525Val
XM_024449167.1:c.1594A>G XP_024304935.1:p.Ile532Val
NM_001032386.2:c.1573A>G MANE Select NP_001027558.1:p.Ile525Val
NM_000456.3:c.1573A>G NP_000447.2:p.Ile525Val
NM_001032387.2:c.1573A>G NP_001027559.1:p.Ile525Val