Human (GRCh37.p13)
Description

hemoglobin, delta [Source:HGNC Symbol;Acc:4829]

Location

Chromosome 11: 5,253,908-5,256,600 reverse strand.

GRCh37:CM000673.1

About this gene

This gene has 4 transcripts (splice variants), 9 paralogues and is associated with 2 phenotypes.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000380299.3HBD-001785147aa
 
Protein coding
CCDS31376A0N071 D1MGP8 D1MGQ0
E9PEW8 P02042 Q5XTR9
NM_000519.3Ensembl CanonicalGENCODE Basic
ENST00000429817.1HBD-004566104aa
 
Protein coding
D1MGP8 E9PEW8 -CDS 3' incomplete
ENST00000292901.3HBD-003486141aa
 
Protein coding
D1MGP8 D1MGQ0 E9PEW8
E9PFT6 Q5XTR9
-GENCODE Basic
ENST00000417377.1HBD-00230585aa
 
Protein coding
C9JRG0 D1MGP8 -CDS 3' incomplete
Name

HBD (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: P02042

CCDS

This gene is a member of the Human CCDS set: CCDS31376.1

Ensembl version

ENSG00000223609.3

Other assemblies

This gene maps to 5,232,678-5,235,370 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000066674 (version 2)

Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Contigs

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