Human (GRCh37.p13)
Description

solute carrier family 16 (monocarboxylate transporter), member 1 [Source:HGNC Symbol;Acc:10922]

Gene Synonyms

HHF7, MCT, MCT1

Location

Chromosome 1: 113,454,469-113,499,635 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 8 transcripts (splice variants), 11 paralogues and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000538576.1SLC16A1-2024374500aaENSP00000441065.1
 
Protein coding
CCDS858P53985 Q5T8R3 Q5T8R4
Q5T8R5
NM_001166496.1GENCODE basic
ENST00000369626.3SLC16A1-0013910500aaENSP00000358640.3
 
Protein coding
CCDS858P53985 Q5T8R3 Q5T8R4
Q5T8R5
NM_003051.3GENCODE basic
ENST00000433570.4SLC16A1-2013117430aaENSP00000445061.1
 
Protein coding
Q49A45 Q5T8R3 Q5T8R4
-GENCODE basic
ENST00000458229.1SLC16A1-0022201456aaENSP00000416167.1
 
Protein coding
Q5T8R3 Q5T8R4 Q5T8R5
-CDS 3' incomplete
ENST00000443580.1SLC16A1-0051099296aaENSP00000399104.1
 
Protein coding
Q5T8R3 Q5T8R4 -CDS 3' incomplete
ENST00000429288.1SLC16A1-003865215aaENSP00000397106.1
 
Protein coding
Q5T8R4 -CDS 3' incomplete
ENST00000478835.1SLC16A1-004452No protein-
 
Processed transcript
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ENST00000481750.1SLC16A1-006430No protein-
 
Processed transcript
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