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_COX_CTG1: 3,340,610-3,356,471 reverse strand.

GRCh38:GL000251.2

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
ENST00000453831.6SLC44A4-2382589710aaENSP00000393939.2
 
Protein coding
Q53GD3-1 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000546461.3SLC44A4-2442634634aaENSP00000449039.1
 
Protein coding
Q53GD3-3 -GENCODE basicTSL:2
ENST00000551168.3SLC44A4-2452505668aaENSP00000448088.1
 
Protein coding
Q53GD3-4 -GENCODE basicTSL:2
ENST00000433046.5SLC44A4-2371233411aaENSP00000404572.1
 
Protein coding
H0Y5I3 -TSL:5CDS 5' and 3' incomplete
ENST00000495620.5SLC44A4-242681No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000482758.5SLC44A4-240426No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000497541.1SLC44A4-243392No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000474603.1SLC44A4-239655No protein-
 
Retained intron
--TSL:3
ENST00000491622.1SLC44A4-241575No protein-
 
Retained intron
--TSL:4