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Human (GRCh37.p13)
Description

transmembrane protein 199 [Source:HGNC Symbol;Acc:18085]

Gene Synonyms

C17orf32, MGC45714

Location

Chromosome 17: 26,684,604-26,708,716 forward strand.

GRCh37:CM000679.1

View alleles of this gene on alternative sequences

About this gene

This gene has 10 transcripts (splice variants), 1 gene allele and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000292114.3TMEM199-0013148208aaENSP00000292114.3
 
Protein coding
CCDS11228J3KS81 K7EJL8 Q8N511
NM_152464.1Ensembl CanonicalGENCODE basic
ENST00000509083.1TMEM199-2011050299aaENSP00000427614.1
 
Protein coding
E9PBQ3 J3KS81 -GENCODE basic
ENST00000395404.3TMEM199-00297134aaENSP00000465232.1
 
Protein coding
K7EJL8 -GENCODE basic
ENST00000555264.2TMEM199-004674125aaENSP00000462356.1
 
Nonsense mediated decay
J3KS81 --
ENST00000580868.1TMEM199-00857889aaENSP00000462195.1
 
Nonsense mediated decay
J3KRW7 --
ENST00000581386.1TMEM199-005481No protein-
 
Processed transcript
---
ENST00000579762.1TMEM199-009385No protein-
 
Processed transcript
---
ENST00000483505.2TMEM199-003735No protein-
 
Retained intron
---
ENST00000577317.1TMEM199-006634No protein-
 
Retained intron
---
ENST00000585027.1TMEM199-007586No protein-
 
Retained intron
---