Human (GRCh38.p14)
Description

solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]

Gene Synonyms

C6ORF29, CTL4, DFNA72, FLJ14491, NG22, TPPT

Location

Scaffold HSCHR6_MHC_SSTO_CTG1: 3,164,419-3,180,268 reverse strand.

GRCh38:GL000256.2

View this gene on the primary assembly.

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000442152.6SLC44A4-2462589710aaENSP00000398852.2
 
Protein coding
Q53GD3 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000553147.1SLC44A4-2542634634aaENSP00000448213.1
 
Protein coding
A0A0G2JL76 -GENCODE basicTSL:2
ENST00000553121.5SLC44A4-2532505668aaENSP00000447704.1
 
Protein coding
Q53GD3 -GENCODE basicTSL:2
ENST00000450933.5SLC44A4-2471233411aaENSP00000400263.1
 
Protein coding
A0A0G2JIN1 -TSL:5CDS 5' and 3' incomplete
ENST00000495181.5SLC44A4-252681No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000467209.5SLC44A4-249426No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000492379.1SLC44A4-250392No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000460923.1SLC44A4-248655No protein-
 
Retained intron
--TSL:3
ENST00000494162.1SLC44A4-251575No protein-
 
Retained intron
--TSL:4