Human (GRCh38.p14)
Description

major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]

Gene Synonyms

D6S222E, RING6

Location

Scaffold HSCHR6_MHC_COX_CTG1: 4,360,810-4,382,925 reverse strand.

GRCh38:GL000251.2

View this gene on the primary assembly.

About this gene

This gene has 10 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000422196.1HLA-DMA-271871290aaENSP00000409144.1
 
Protein coding
A0A140T9N9 -Ensembl CanonicalTSL:NACDS 5' and 3' incomplete
ENST00000453490.6HLA-DMA-2741126261aaENSP00000404018.2
 
Protein coding
P28067 Q31604 Q6ICR9
-GENCODE basicTSL:NA
ENST00000451148.6HLA-DMA-2721010227aaENSP00000414016.2
 
Protein coding
Q5SP00 -GENCODE basicTSL:NA
ENST00000452703.6HLA-DMA-273780166aaENSP00000405208.2
 
Protein coding
A2AAT8 -GENCODE basicTSL:NA
ENST00000416297.1HLA-DMA-270611169aaENSP00000398728.1
 
Protein coding
A0A140T9C7 -TSL:NACDS 3' incomplete
ENST00000466446.1HLA-DMA-276806No protein-
 
Protein coding CDS not defined
--TSL:NA
ENST00000493659.5HLA-DMA-279698No protein-
 
Protein coding CDS not defined
--TSL:NA
ENST00000481354.1HLA-DMA-2781738No protein-
 
Retained intron
--TSL:NA
ENST00000475284.1HLA-DMA-277984No protein-
 
Retained intron
--TSL:NA
ENST00000460128.5HLA-DMA-275660No protein-
 
Retained intron
--TSL:NA