Human (GRCh37.p13)
Description

transferrin [Source:HGNC Symbol;Acc:11740]

Gene Synonyms

PRO1557, PRO2086, TFQTL1

Location

Chromosome 3: 133,464,800-133,497,850 forward strand.

GRCh37:CM000665.1

About this gene

This gene has 15 transcripts (splice variants), 2 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000402696.3TF-0012968698aaENSP00000385834.3
 
Protein coding
CCDS3080B4DEX9 C9JB55 C9JVG0
J3KN47 P02787
NM_001063.3GENCODE basic
ENST00000264998.3TF-2012143571aaENSP00000264998.3
 
Protein coding
C9JVG0 J3KN47 -GENCODE basic
ENST00000482271.1TF-008659134aaENSP00000419338.1
 
Protein coding
C9JVG0 -CDS 3' incomplete
ENST00000466911.1TF-01652675aaENSP00000417468.1
 
Protein coding
C9JB55 -CDS 3' incomplete
ENST00000461695.1TF-014990143aaENSP00000419714.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000494430.1TF-013594120aaENSP00000418396.1
 
Nonsense mediated decay
F8WCI6 --
ENST00000485977.1TF-011580102aaENSP00000418716.1
 
Nonsense mediated decay
F8WC57 --
ENST00000414694.1TF-006546115aaENSP00000401505.1
 
Nonsense mediated decay
F8WEK9 --
ENST00000475382.1TF-010586No protein-
 
Processed transcript
---
ENST00000467842.1TF-0044602No protein-
 
Retained intron
---
ENST00000493011.1TF-017999No protein-
 
Retained intron
---
ENST00000498622.1TF-012719No protein-
 
Retained intron
---
ENST00000474287.1TF-005645No protein-
 
Retained intron
---
ENST00000462495.1TF-007582No protein-
 
Retained intron
---
ENST00000460531.1TF-009577No protein-
 
Retained intron
---