Human (GRCh38.p14) ▼ 
Summary
SequenceProtein InformationGenetic VariationVariant tableVariant imageHaplotypesPopulation comparisonComparison imageExternal ReferencesSupporting evidenceID History.
solute carrier family 46 member 3 [Source:HGNC Symbol;Acc:HGNC:27501]
DKFZP686A1775, FLJ42613
Chromosome 13: 28,700,080-28,718,970 reverse strand.
This transcript has 6 exons, is annotated with 21 domains and features, is associated with 7818 variant alleles and maps to 419 oligo probes.
This transcript is a product of gene ENSG00000139508.15 Show transcript tableHide transcript table
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Exons: 6, Coding exons: 5, Transcript length: 3,302 bps, Translation length: 461 residues
This MANE Select transcript contains ENSP00000266943 and matches to NM_181785.4 and NP_861450.1
This transcript corresponds to the following Uniprot identifiers: Q7Z3Q1
This transcript is a member of the Human CCDS set: CCDS9332
TSL:1
ENST00000266943.11
Protein coding
Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.
This transcript is a member of the Gencode basic gene set.
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Ensembl release 111 - January 2024 ©
EMBL-EBI
EMBL-EBI
http://useast.ensembl.org
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