Canonical Allele Identifier: CA261429
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43551
dbSNP Id: rs111033241

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107663425_107663429del , CM000669.2:g.107663425_107663429del GRCh38
NC_000007.13:g.107303870_107303874del , CM000669.1:g.107303870_107303874del GRCh37
NC_000007.12:g.107091106_107091110del NCBI36
NG_008489.1:g.7791_7795del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.294_298del MANE Select ENSP00000494017.1:p.Thr99AlafsTer?
ENST00000265715.7:c.294_298del ENSP00000265715.3:p.Thr99AlafsTer?
ENST00000440056.1:c.294_298del ENSP00000394760.1:p.Thr99AlafsTer?
NM_000441.1:c.294_298del NP_000432.1:p.Thr99AlafsTer?
XM_005250425.1:c.294_298del XP_005250482.1:p.Thr99AlafsTer?
XM_006716025.2:c.294_298del XP_006716088.1:p.Thr99AlafsTer?
XM_005250425.2:c.294_298del XP_005250482.1:p.Thr99AlafsTer?
XM_006716025.3:c.294_298del XP_006716088.1:p.Thr99AlafsTer?
XM_017012318.1:c.294_298del XP_016867807.1:p.Thr99AlafsTer?
NM_000441.2:c.294_298del MANE Select NP_000432.1:p.Thr99AlafsTer?