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Human (GRCh38.p14)
Description

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

Gene Synonyms

MCT, MCT1

Location

Scaffold HG2104_PATCH: 2,426-47,592 reverse strand.

GRCh38:KN196474.1

View this gene on the primary assembly.

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000628110.2SLC16A1-2264374500aaENSP00000485688.1
 
Protein coding
P53985-1 -Ensembl CanonicalGENCODE PrimaryGENCODE Basic
ENST00000630362.4SLC16A1-2293910500aaENSP00000486000.1
 
Protein coding
P53985-1 -GENCODE Basic
ENST00000629920.2SLC16A1-2282201456aaENSP00000486874.1
 
Protein coding
Q5T8R5 -CDS 3' incomplete
ENST00000629508.2SLC16A1-2271099296aaENSP00000486404.1
 
Protein coding
Q5T8R3 -CDS 3' incomplete
ENST00000626371.1SLC16A1-223865215aaENSP00000485854.1
 
Protein coding
Q5T8R4 -CDS 3' incomplete
ENST00000627457.1SLC16A1-225452No protein-
 
Protein coding CDS not defined
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ENST00000627031.1SLC16A1-224430No protein-
 
Protein coding CDS not defined
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