Human (GRCh37.p13)
Description

solute carrier family 48 (heme transporter), member 1 [Source:HGNC Symbol;Acc:26035]

Gene Synonyms

FLJ20489, HRG-1, HRG1, hHRG-1

Location

Chromosome 12: 48,147,699-48,176,536 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 9 transcripts (splice variants) and 260 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000442218.2SLC48A1-0013010146aaENSP00000415998.2
 
Protein coding
CCDS8755F8VQX9 Q6P1K1 NM_017842.2Ensembl CanonicalGENCODE Basic
ENST00000442892.2SLC48A1-002102489aaENSP00000410134.2
 
Protein coding
F8VQX9 Q6P1K1 -GENCODE Basic
ENST00000547002.1SLC48A1-00775189aaENSP00000446739.1
 
Protein coding
F8VQX9 Q6P1K1 -GENCODE Basic
ENST00000548498.1SLC48A1-00861836aaENSP00000450234.1
 
Protein coding
F8VQX9 -CDS 3' incomplete
ENST00000549243.1SLC48A1-00957716aaENSP00000446686.1
 
Protein coding
--CDS 3' incomplete
ENST00000551301.1SLC48A1-006107052aaENSP00000449036.1
 
Nonsense mediated decay
F8VXV4 --
ENST00000476104.1SLC48A1-005567No protein-
 
Processed transcript
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ENST00000461620.1SLC48A1-004459No protein-
 
Processed transcript
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ENST00000552003.1SLC48A1-010882No protein-
 
Retained intron
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