Human (GRCh38.p14)
Description

solute carrier family 44 member 1 [Source:HGNC Symbol;Acc:HGNC:18798]

Gene Synonyms

CD92, CDW92, CHTL1, CTL1

Location

Chromosome 9: 105,244,622-105,439,171 forward strand.

GRCh38:CM000671.2

About this gene

This gene has 9 transcripts (splice variants), 268 orthologues, 4 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000374720.8SLC44A1-20110482657aaENSP00000363852.3
 
Protein coding
CCDS6763Q8WWI5-1 NM_080546.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000374723.5SLC44A1-2029640652aaENSP00000363855.1
 
Protein coding
CCDS75868Q8WWI5-3 -GENCODE basicTSL:1
ENST00000699289.1SLC44A1-2083516724aaENSP00000514270.1
 
Protein coding
A0A8V8TN05 -GENCODE basic
ENST00000374724.1SLC44A1-2033088654aaENSP00000363856.1
 
Protein coding
CCDS83390Q8WWI5-2 -GENCODE basicTSL:5
ENST00000699290.1SLC44A1-2092749726aaENSP00000514271.1
 
Protein coding
A0A8V8TN34 -GENCODE basic
ENST00000470972.5SLC44A1-20510433657aaENSP00000433072.1
 
Nonsense mediated decay
CCDS6763Q8WWI5-1 -TSL:1
ENST00000607692.1SLC44A1-206586No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000436716.1SLC44A1-204576No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000607701.1SLC44A1-207558No protein-
 
Retained intron
--TSL:4