Canonical Allele Identifier: CA947976685
Gene: SUOX HGNC NCBI

Linked Data

dbSNP Id: rs1890614602

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56003642_56003643del , CM000674.2:g.56003642_56003643del GRCh38
NC_000012.11:g.56397426_56397427del , CM000674.1:g.56397426_56397427del GRCh37
NC_000012.10:g.54683693_54683694del NCBI36
NG_008136.1:g.11384_11385del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266971.8:c.253_254del MANE Select ENSP00000266971.3:p.Tyr85HisfsTer2
ENST00000266971.7:c.253_254del ENSP00000266971.3:p.Tyr85HisfsTer2
ENST00000356124.8:c.253_254del ENSP00000348440.4:p.Tyr85HisfsTer2
ENST00000394109.7:c.253_254del ENSP00000377668.3:p.Tyr85HisfsTer2
ENST00000394115.6:c.253_254del ENSP00000377674.2:p.Tyr85HisfsTer2
ENST00000546712.1:n.744_745del
ENST00000546833.5:c.253_254del ENSP00000449872.1:p.Tyr85HisfsTer2
ENST00000548274.5:c.253_254del ENSP00000450245.1:p.Tyr85HisfsTer2
ENST00000550065.1:c.253_254del ENSP00000450264.1:p.Tyr85HisfsTer2
ENST00000550340.5:n.138_139del
ENST00000550478.5:n.332_333del
ENST00000551698.5:n.275_276del
ENST00000551841.6:c.253_254del ENSP00000449443.1:p.Tyr85HisfsTer2
ENST00000552258.5:c.253_254del ENSP00000450049.1:p.Tyr85HisfsTer2
ENST00000552363.5:n.106_107del
NM_000456.2:c.253_254del NP_000447.2:p.Tyr85HisfsTer2
NM_001032386.1:c.253_254del NP_001027558.1:p.Tyr85HisfsTer2
NM_001032387.1:c.253_254del NP_001027559.1:p.Tyr85HisfsTer2
XM_005269112.1:c.274_275del XP_005269169.1:p.Tyr92HisfsTer2
XM_017019905.2:c.274_275del XP_016875394.1:p.Tyr92HisfsTer2
XM_017019906.1:c.274_275del XP_016875395.1:p.Tyr92HisfsTer2
XM_017019907.2:c.253_254del XP_016875396.1:p.Tyr85HisfsTer2
XM_017019908.1:c.253_254del XP_016875397.1:p.Tyr85HisfsTer2
XM_024449167.1:c.274_275del XP_024304935.1:p.Tyr92HisfsTer2
NM_001032386.2:c.253_254del MANE Select NP_001027558.1:p.Tyr85HisfsTer2
NM_000456.3:c.253_254del NP_000447.2:p.Tyr85HisfsTer2
NM_001032387.2:c.253_254del NP_001027559.1:p.Tyr85HisfsTer2