Canonical Allele Identifier: CA2619252524
Gene: SUOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56003786del , CM000674.2:g.56003786del GRCh38
NC_000012.11:g.56397570del , CM000674.1:g.56397570del GRCh37
NC_000012.10:g.54683837del NCBI36
NG_008136.1:g.11528del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266971.8:c.397del MANE Select ENSP00000266971.3:p.Leu133Ter
ENST00000266971.7:c.397del ENSP00000266971.3:p.Leu133Ter
ENST00000356124.8:c.397del ENSP00000348440.4:p.Leu133Ter
ENST00000394109.7:c.397del ENSP00000377668.3:p.Leu133Ter
ENST00000394115.6:c.397del ENSP00000377674.2:p.Leu133Ter
ENST00000546833.5:c.397del ENSP00000449872.1:p.Leu133Ter
ENST00000548274.5:c.397del ENSP00000450245.1:p.Leu133Ter
ENST00000550065.1:c.397del ENSP00000450264.1:p.Leu133Ter
ENST00000550340.5:n.282del
ENST00000550478.5:n.476del
ENST00000551698.5:n.419del
ENST00000551841.6:c.267+130del ENSP00000449443.1:n.267+130del
ENST00000552363.5:n.250del
NM_000456.2:c.397del NP_000447.2:p.Leu133Ter
NM_001032386.1:c.397del NP_001027558.1:p.Leu133Ter
NM_001032387.1:c.397del NP_001027559.1:p.Leu133Ter
XM_005269112.1:c.418del XP_005269169.1:p.Leu140Ter
XM_017019905.2:c.418del XP_016875394.1:p.Leu140Ter
XM_017019906.1:c.418del XP_016875395.1:p.Leu140Ter
XM_017019907.2:c.397del XP_016875396.1:p.Leu133Ter
XM_017019908.1:c.397del XP_016875397.1:p.Leu133Ter
XM_024449167.1:c.418del XP_024304935.1:p.Leu140Ter
NM_001032386.2:c.397del MANE Select NP_001027558.1:p.Leu133Ter
NM_000456.3:c.397del NP_000447.2:p.Leu133Ter
NM_001032387.2:c.397del NP_001027559.1:p.Leu133Ter