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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_MCF_CTG1: 3,205,262-3,221,111 reverse strand.

GRCh38:GL000254.2

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
ENST00000415517.6SLC44A4-2342589710aaENSP00000414120.2
 
Protein coding
Q53GD3 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000547288.5SLC44A4-2412634634aaENSP00000446935.1
 
Protein coding
A0A0G2JL76 -GENCODE BasicTSL:2
ENST00000547493.1SLC44A4-2422505668aaENSP00000449232.1
 
Protein coding
Q53GD3 -GENCODE BasicTSL:2
ENST00000441920.5SLC44A4-2351233411aaENSP00000414296.1
 
Protein coding
A0A0G2JIN1 -TSL:5CDS 5' and 3' incomplete
ENST00000463111.5SLC44A4-238681No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000485731.5SLC44A4-240426No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000459749.1SLC44A4-236392No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000460693.1SLC44A4-237655No protein-
 
Retained intron
--TSL:3
ENST00000481664.1SLC44A4-239575No protein-
 
Retained intron
--TSL:4