Human (GRCh37.p13)
Description

solute carrier family 26, member 10 [Source:HGNC Symbol;Acc:14470]

Location

Chromosome 12: 58,013,310-58,019,934 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 10 transcripts (splice variants).

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000320442.4SLC26A10-0012389563aaENSP00000320217.4
 
Protein coding
CCDS8949Q8NG04 NM_133489.2Ensembl CanonicalGENCODE Basic
ENST00000379218.2SLC26A10-2012515454aaENSP00000368520.2
 
Protein coding
Q8NG04 -GENCODE Basic
ENST00000474359.2SLC26A10-0102173520aaENSP00000431994.1
 
Nonsense mediated decay
E9PIH7 --
ENST00000440686.1SLC26A10-0031819412aaENSP00000403619.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000490243.1SLC26A10-006663No protein-
 
Processed transcript
---
ENST00000483647.1SLC26A10-004501No protein-
 
Processed transcript
---
ENST00000487816.1SLC26A10-0021794No protein-
 
Retained intron
---
ENST00000474791.1SLC26A10-005715No protein-
 
Retained intron
---
ENST00000497297.1SLC26A10-008586No protein-
 
Retained intron
---
ENST00000463802.1SLC26A10-009577No protein-
 
Retained intron
---