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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_APD_CTG1: 3,195,808-3,211,661 reverse strand.

GRCh38:GL000250.2

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
ENST00000417894.6SLC44A4-2622589710aaENSP00000389244.2
 
Protein coding
Q53GD3 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000550821.4SLC44A4-2692634634aaENSP00000450005.1
 
Protein coding
A0A0G2JL76 -GENCODE BasicTSL:2
ENST00000550401.2SLC44A4-2682505668aaENSP00000448474.1
 
Protein coding
Q53GD3 -GENCODE BasicTSL:2
ENST00000414684.5SLC44A4-2611233411aaENSP00000415708.1
 
Protein coding
A0A0G2JIN1 -TSL:5CDS 5' and 3' incomplete
ENST00000492911.5SLC44A4-267681No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000473048.5SLC44A4-263426No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000487052.1SLC44A4-265392No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000488616.1SLC44A4-266655No protein-
 
Retained intron
--TSL:3
ENST00000484190.1SLC44A4-264575No protein-
 
Retained intron
--TSL:5