Human (GRCh38.p14)
Description

solute carrier family 46 member 1 [Source:HGNC Symbol;Acc:HGNC:30521]

Gene Synonyms

HCP1, HPCFT, HSPCFT, MGC9564, PCFT

Location

Chromosome 17: 28,394,642-28,407,197 reverse strand.

GRCh38:CM000679.2

About this gene

This gene has 9 transcripts (splice variants), 204 orthologues, 2 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000612814.5SLC46A1-2076492459aaENSP00000480703.1
 
Protein coding
CCDS74020Q96NT5-1 NM_080669.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000618626.1SLC46A1-2085363431aaENSP00000483652.1
 
Protein coding
CCDS74019Q96NT5-2 -GENCODE basicTSL:1
ENST00000584995.5SLC46A1-2061030250aaENSP00000464190.1
 
Protein coding
J3QRF7 -TSL:3CDS 3' incomplete
ENST00000581516.1SLC46A1-20284432aaENSP00000462942.1
 
Protein coding
J3KTE6 -TSL:5CDS 3' incomplete
ENST00000582735.1SLC46A1-204574124aaENSP00000463339.1
 
Protein coding
J3QL21 -TSL:4CDS 5' incomplete
ENST00000584426.1SLC46A1-205564128aaENSP00000467416.1
 
Protein coding
K7EPJ7 -TSL:4CDS 3' incomplete
ENST00000578217.1SLC46A1-201596No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000582590.1SLC46A1-2031435No protein-
 
Retained intron
--TSL:2
ENST00000619923.1SLC46A1-209528No protein-
 
Retained intron
--TSL:NA