Human (GRCh38.p14)
Description

solute carrier family 16 member 1 [Source:HGNC Symbol;Acc:HGNC:10922]

Gene Synonyms

MCT, MCT1

Location

Chromosome 1: 112,911,847-112,957,593 reverse strand.

GRCh38:CM000663.2

View alleles of this gene on alternative sequences

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele, 340 orthologues, 13 paralogues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000369626.8SLC16A1-2013753500aaENSP00000358640.4
 
Protein coding
CCDS858P53985-1 NM_003051.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000538576.5SLC16A1-2074374500aaENSP00000441065.1
 
Protein coding
CCDS858P53985-1 -APPRIS P1TSL:2
ENST00000458229.6SLC16A1-2043849500aaENSP00000416167.2
 
Protein coding
CCDS858P53985-1 -APPRIS P1TSL:2
ENST00000443580.6SLC16A1-2033764500aaENSP00000399104.2
 
Protein coding
CCDS858P53985-1 -APPRIS P1TSL:3
ENST00000429288.2SLC16A1-2023757500aaENSP00000397106.2
 
Protein coding
CCDS858P53985-1 -APPRIS P1TSL:3
ENST00000679803.1SLC16A1-2083647500aaENSP00000505879.1
 
Protein coding
CCDS858P53985-1 -APPRIS P1
ENST00000478835.1SLC16A1-205452No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000481750.1SLC16A1-206430No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000679846.1SLC16A1-2093117No protein-
 
Retained intron
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