Human (GRCh38.p14)
Description

serine hydroxymethyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10850]

Gene Synonyms

CSHMT, MGC15229, MGC24556, SHMT

Location

Scaffold HSCHR17_3_CTG1: 88,247-123,941 reverse strand.

GRCh38:KV766198.1

View this gene on the primary assembly.

About this gene

This gene has 9 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000640392.2SHMT1-2102519483aaENSP00000492715.2
 
Protein coding
P34896-1 -Ensembl CanonicalGENCODE basic
ENST00000711529.1SHMT1-2122469483aaENSP00000518786.1
 
Protein coding
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ENST00000711531.1SHMT1-2141656444aaENSP00000518788.1
 
Protein coding
--GENCODE basic
ENST00000711534.1SHMT1-217880167aaENSP00000518789.1
 
Protein coding
--CDS 3' incomplete
ENST00000711530.1SHMT1-2131759128aaENSP00000518787.1
 
Nonsense mediated decay
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ENST00000711532.1SHMT1-2152756No protein-
 
Retained intron
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ENST00000711528.1SHMT1-2112652No protein-
 
Retained intron
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ENST00000711533.1SHMT1-2161077No protein-
 
Retained intron
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ENST00000711535.1SHMT1-218570No protein-
 
Retained intron
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