Human (GRCh38.p14)
Description

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

Gene Synonyms

CSHMT, MGC15229, MGC24556, SHMT

Location

Chromosome 17: 18,327,873-18,363,550 reverse strand.

GRCh38:CM000679.2

View alleles of this gene on alternative sequences

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele, 207 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000316694.8SHMT1-2012527483aaENSP00000318868.3
 
Protein coding
CCDS11196P34896-1 NM_004169.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000583780.2SHMT1-2092469483aaENSP00000462041.2
 
Protein coding
CCDS11196--APPRIS P1TSL:1
ENST00000354098.7SHMT1-2021656444aaENSP00000318805.3
 
Protein coding
CCDS11197P34896-2 -GENCODE basicTSL:1
ENST00000582653.1SHMT1-208879167aaENSP00000462227.1
 
Protein coding
J3KRZ5 -TSL:3CDS 3' incomplete
ENST00000580002.5SHMT1-2061759128aaENSP00000462043.1
 
Nonsense mediated decay
J3KRK5 -TSL:2
ENST00000582352.1SHMT1-2072756No protein-
 
Retained intron
--TSL:NA
ENST00000395684.5SHMT1-2042652No protein-
 
Retained intron
--TSL:1
ENST00000579558.5SHMT1-2051077No protein-
 
Retained intron
--TSL:2
ENST00000395682.3SHMT1-203570No protein-
 
Retained intron
--TSL:2